Receptors and membrane-associated proteins

ABSTRACT

The invention provides human receptors and membrane-associated proteins (REMAP) and polynucleotides which identify and encode REMAP. The invention also provides expression vectors, host cells, antibodies, agonists, and antagonists. The invention also provides methods for diagnosing, treating, or preventing disorders associated with aberrant expression of REMAP.

TECHNICAL FIELD

[0001] This invention relates to nucleic acid and amino acid sequences of receptors and membrane-associated proteins and to the use of these sequences in the diagnosis, treatment, and prevention of cardiovascular, neurological, gastrointestinal, lipid metabolism, cell proliferative, autoimmune/inflammatory, metabolic, developmental, and endocrine disorders, and in the assessment of the effects of exogenous compounds on the expression of nucleic acid and amino acid sequences of receptors and membrane-associated proteins.

BACKGROUND OF THE INVENTION

[0002] Eukaryotic organisms are distinct from prokaryotes in possessing many intracellular membrane-bound compartments such as organelles and vesicles. Many of the metabolic reactions which distinguish eukaryotic biochemistry from prokaryotic biochemistry take place within these compartments. In particular, many cellular functions require very stringent reaction conditions, and the organelles and vesicles enable compartmentalization and isolation of reactions which might otherwise disrupt cytosolic metabolic processes. The organelles include mitochondria, smooth and rough endoplasmic reticular sarcoplasmic reticulum, and the Golgi body. The vesicles include phagosomes, lysosomes, endosomes, peroxisomes, and secretory vesicles. Organelles and vesicles are bounded by single or double membranes.

[0003] Biological membranes surround organelles, vesicles, and the cell itself. Membranes are highly selective permeability barriers made up of lipid bilayer sheets composed of phosphoglycerides, fatty acids, cholesterol, phospholipids, glycolipids, proteoglycans, and proteins. Membranes contain ion pumps, ion channels, and specific receptors for external stimuli which transmit biochemical signals across the membranes. These membranes also contain second messenger proteins which interact with these pumps, channels, and receptors to amplify and regulate transmission of these signals.

[0004] Plasma Membrane Proteins

[0005] Transmembrane proteins (TM) are characterized by extracellular, transmembrane, and intracellular domains. TM domains are typically comprised of 15 to 25 hydrophobic amino acids which are predicted to adopt an α-helical conformation. TM proteins are classified as bitopic (Types I and II) proteins, which span the membrane once, and polytopic (Types III and IV) (Singer, S. J. (1990) Annu. Rev. Cell Biol. 6:247-96) proteins, which contain multiple membrane-spanning segments. TM proteins that act as cell-surface receptor proteins involved in signal transduction include growth and differentiation factor receptors, and receptor-interacting proteins such as Drosophila pecanex and frizzled proteins, LIV-1 protein, NF2 protein, and GNS1/SUR4 eukaryotic integral membrane proteins. TM proteins also act as transporters of ions or metabolites, such as gap junction channels (connexins) and ion channels, and as cell anchoring proteins, such as lectins, integrins, and fibronectins. TM proteins function as vesicle and organelle-forming molecules, such as calveolins; or cell recognition molecules, such as cluster of differentiation (CD) antigens, glycoproteins, and mucins.

[0006] The transport of hydrophilic molecules across membranes is facilitated by the presence of channel proteins which form aqueous pores which can perforate a lipid bilayer. Many channels consist of protein complexes formed by the assembly of multiple subunits, at least one of which is an integral membrane protein that contributes to formation of the pore. In some cases, the pore is constructed to allow selective passage of only one or a few molecular species. Distinct types of membrane channels that differ greatly in their distribution and selectivity include: (1) aquaporins, which transport water; (2) protein-conducting channels, which transport proteins across the endoplasmic reticulum membrane; (3) gap junctions, which facilitate diffusion of ions and small organic molecules between neighboring cells; and (4) ion channels, which regulate ion flux through various membranes.

[0007] Many membrane proteins (MPs) contain amino acid sequence motifs that serve to localize proteins to specific subcellular sites. Examples of these motifs include PDZ domains, KDEL, RGD, NGR, and GSL sequence motifs, von Willebrand factor A (vWFA) domains, and EGF-like domains. RGD, NGR, and GSL motif-containing peptides have been used as drug delivery agents in targeted cancer treatment of tumor vasculature (Arap, W. et al. (1998) Science, 279:377-380). Membrane proteins may also contain amino acid sequence motifs that serve to interact with extracellular or intracellular molecules, such as carbohydrate recognition domains.

[0008] Chemical modification of amino acid residue side chains alters the manner in which MPs interact with other molecules, such as membrane phospholipids. Examples of such chemical modifications include the formation of covalent bonds with glycosaminoglycans, oligosaccharides, phospholipids, acetyl and palmitoyl moieties, ADP-ribose, phosphate, and sulphate groups.

[0009] RNA encoding membrane proteins may have alternative splice sites which give rise to proteins encoded by the same gene but with different messenger RNA and amino acid sequences. Splice variant membrane proteins may interact with other ligand and protein isoforms.

[0010] Receptors

[0011] The term receptor describes proteins that specifically recognize other molecules. The category is broad and includes proteins with a variety of functions. The bulk of receptors are cell surface proteins which bind extracellular ligands and produce cellular responses in the areas of growth, differentiation, endocytosis, and immune response. Other receptors facilitate the selective transport of proteins out of the endoplasmic reticulum and localize enzymes to particular locations in the cell. The term may also be applied to proteins which act as receptors for ligands with known or unknown chemical composition and which interact with other cellular components. For example, the steroid hormone receptors bind to and regulate transcription of DNA.

[0012] G-Protein Coupled Receptors

[0013] G-protein coupled receptors (GPCR) comprise a superfamily of integral membrane proteins which transduce extracellular signals. GPCRs include receptors for biogenic amines, lipid mediators of inflammation, peptide hormones, and sensory signal mediators.

[0014] The structure of these highly-conserved receptors consists of seven hydrophobic transmembrane regions, an extracellular N-terminus, and a cytoplasmic C-terminus. Three extracellular loops alternate with three intracellular loops to link the seven transmembrane regions. The most conserved parts of these proteins are the transmembrane regions and the first two cytoplasmic loops. Cysteine disulfide bridges connect the second and third extracellular loops. A conserved, acidic-Arg-aromatic residue triplet present in the second cytoplasmic loop may interact with G proteins. A GPCR consensus pattern is characteristic of most proteins belonging to this superfamily (ExPASy PROSITE document PS00237; and Watson, S. and S. Arkinstall (1994) The G-protein Linked Receptor Facts Book, Academic Press, San Diego, Calif., pp 2-6). Mutations and changes in transcriptional activation of GPCR-encoding genes have been associated with neurological disorders such as schizophrenia, Parkinson's disease, Alzheimer's disease, drug addiction, and feeding disorders.

[0015] Scavenger Receptors

[0016] Macrophage scavenger receptors with broad ligand specificity may participate in the binding of low density lipoproteins (LDL) and foreign antigens. Scavenger receptors types I and II are trimeric membrane proteins with each subunit containing a small N-terminal intracellular domain, a transmembrane domain, a large extracellular domain, and a C-terminal cysteine-rich domain. The extracellular domain contains a short spacer domain, an α-helical coiled-coil domain, and a triple helical collagenous domain. These receptors have been shown to bind a spectrum of ligands, including chemically modified lipoproteins and albumin, polyribonucleotides, polysaccharides, phospholipids, and asbestos (Matsumoto, A. et al. (1990) Proc. Natl. Acad. Sci. 87:9133-9137; and Elomaa, O. et al. (1995) Cell 80:603-609). The scavenger receptors are thought to play a key role in atherogenesis by mediating uptake of modified LDL in arterial walls, and in host defense by binding bacterial endotoxins, bacteria, and protozoa.

[0017] Tetraspan Family Proteins

[0018] The transmembrane 4 superfamily (TM4SF), or tetraspan family, is a multigene family encoding type III integral membrane proteins (Wright, M. D. and Tomlinson, M. G. (1994) Inmunol. Today 15:588-594). TM4SF is comprised of membrane proteins which traverse the cell membrane four times. Members of the TM4SF include platelet and endothelial cell membrane proteins, melanoma-associated antigens, leukocyte surface glycoproteins, colonal carcinoma antigens, tumor-associated antigens, and surface proteins of the schistosome parasites (Jankowski, S. A. (1994) Oncogene 9:1205-1211). Members of the TM4SF share about 25-30% amino acid sequence identity with one another.

[0019] A number of TM4SF members have been implicated in signal transduction, control of cell adhesion, regulation of cell growth and proliferation, including development and oncogenesis, and cell motility, including tumor cell metastasis. Expression of TM4SF proteins is associated with a variety of tumors, and the level of expression may be altered when cells are growing or activated.

[0020] Tumor Antigens

[0021] Tumor antigens are surface molecules that are differentially expressed in tumor cells relative to normal cells. Tumor antigens distinguish tumor cells immunologically from normal cells and provide diagnostic and therapeutic targets for human cancers (Takagi, S. et al. (1995) Int. J. Cancer 61: 706-715; Liu, E. et al. (1992) Oncogene 7: 1027-1032).

[0022] Ion Channels

[0023] Ion channels are found in the plasma membranes of virtually every cell in the body. For example, chloride channels mediate a variety of cellular functions including regulation of membrane potential and absorption and secretion of ions across epithelial membranes. When present in intracellular membranes of the Golgi apparatus and endocytic vesicles, chloride channels also regulate organelle pH (see, e.g., Greger, R. (1988) Annu. Rev. Physiol. 50:111-122). Electrophysiological and pharmacological properties of chloride channels, including ion conductance, current-voltage relationships, and sensitivity to modulators, suggest that different chloride channels exist in muscles, neurons, fibroblasts, epithelial cells, and lymphocytes.

[0024] Many channels have sites for phosphorylation by one or more protein kinases including protein kinase A, protein kinase C, casein kinase II, and tyrosine kinases, all of which regulate ion channel activity in cells. Inappropriate phosphorylation of membrane proteins has been correlated with pathological changes in cell cycle progression and cell differentiation. Changes in the cell cycle have been linked to induction of apoptosis or cancer. Changes in cell differentiation have been linked to diseases and disorders of the reproductive system, immune system, and skeletal muscle.

[0025] Proton Pumps

[0026] Proton ATPases are a large class of membrane proteins that use the energy of ATP hydrolysis to generate an electrochemical proton gradient across a membrane. The resultant gradient may be used to transport other ions across the membrane (Na⁺, K⁺, or Cl⁻) or to maintain organelle pH. Proton ATPases are further subdivided into the mitochondrial F-ATPases, the plasma membrane ATPases, and the vacuolar ATPases. The vacuolar ATPases establish and maintain an acidic pH within various vesicles involved in the processes of endocytosis and exocytosis (Mellman, I. et al. (1986) Ann. Rev. Biochem. 55:663-700).

[0027] Proton-coupled, 12 membrane-spanning domain transporters such as PEPT 1 and PEPT 2 are responsible for gastrointestinal absorption and for renal reabsorption of peptides using an electrochemical H⁺ gradient as the driving force. Another type of peptide transporter, the TAP transporter, is a heterodimer consisting of TAP 1 and TAP 2 and is associated with antigen processing. Peptide antigens are transported across the membrane of the endoplasmic reticulum by TAP so they can be expressed on the cell surface in association with MHC molecules. Each TAP protein consists of multiple hydrophobic membrane spanning segments and a highly conserved ATP-binding cassette (Boll M. et al (1996) Proc. Natl. Acad. Sci. 93:284-289). Pathogenic microorganisms, such as herpes simplex virus, may encode inhibitors of TAP-mediated peptide transport in order to evade immune surveillance (Marusina, K. and Manaco, J. J. (1996) Curr. Opin. Hematol 3:19-26).

[0028] ABC Transporters

[0029] The ATP-binding cassette (ABC) transporters, also called the “traffic ATPases”, comprise a superfamily of membrane proteins that mediate transport and channel functions in prokaryotes and eukaryotes (Higgins, C. F. (1992) Annu. Rev. Cell Biol. 8:67-113). ABC proteins share a similar overall structure and significant sequence homology. All ABC proteins contain a conserved domain of approximately two hundred amino acid residues which includes one or more nucleotide binding domains. Mutations in ABC transporter genes are associated with various disorders, such as hyperbilirubinemia II/Dubin-Johnson syndrome, recessive Stargardt's disease, X-linked adrenoluekodystrophy, multidrug resistance, celiac disease, and cystic librosis.

[0030] Cell Adhesion Proteins The surface of a cell is rich in transmembrane proteoglycans, glycoproteins, glycolipids, and receptors. These macromolecules mediate adhesion with other cells and with components of the ECM. The interaction of the cell with its surroundings profoundly influences cell shape, strength, flexibility, motility, and adhesion. These dynamic properties are intimately associated with signal transduction pathways controlling cell proliferation and differentiation, tissue construction, and embryonic development. Families of cell adhesion molecules include the cadherins, integrins, lectins, neural cell adhesion proteins, and some members of the proline-rich proteins.

[0031] Vezatin is a ubiquitous protein of adherens cell-cell junctions, where it interacts with both myosin VIIA and the cadherin-catenins complex (Kussel-Andermann, P. et al. (2000) EMBO J. 19:6020-6029).

[0032] Semaphorins and Neuropilins

[0033] Semaphorins are a large group of axonal guidance molecules consisting of at least 30 different members and are found in vertebrates, invertebrates, and even certain viruses. All semaphorins contain the sema domain which is approximately 500 amino acids in length. Neuropilin, a semaphorin receptor, has been shown to promote neurite outgrowth in vitro. The extracellular region of neuropilins consists of three different domains: CUB, discoidin, and MAM domains. The CUB and the MAM motifs of neuropilin have been suggested to have roles in protein-protein interactions and are thought to be involved in the binding of semaphorins through the sema and the C-terminal domains (reviewed in Raper, J. A. (2000) Curr. Opin. Neurobiol. 10:88-94).

[0034] Membrane Proteins Associated with Intercellular Communication

[0035] Intercellular communication is essential for the development and survival of multicellular organisms. Cells communicate with one another through the secretion and uptake of protein signaling molecules. The uptake of proteins into the cell is achieved by endocytosis, in which the interaction of signaling molecules with the plasma membrane surface, often via binding to specific receptors, results in the formation of plasma membrane-derived vesicles that enclose and transport the molecules into the cytosol. The secretion of proteins from the cell is achieved by exocytosis, in which molecules inside of the cell are packaged into membrane-bound transport vesicles derived from the trans Golgi network. These vesicles fuse with the plasma membrane and release their contents into the surrounding extracellular space. Endocytosis and exocytosis result in the removal and addition of plasma membrane components, and the recycling of these components is essential to maintain the integrity, identity, and functionality of both the plasma membrane and internal memnbrane-bound compartments.

[0036] Lipid rafts are microdomains of the plasma membrane enriched in cholesterol and sphingolipids. These regions concentrate certain signaling molecules, including heterotrimeric and small G proteins, Src-family tyrosine kinases, endothelial nitric oxide synthase, G-protein-coupled receptors, and certain tyrosine kinase receptors. This concentration of signaling molecules suggests that these microdomains might function as a site for compartmentalization of signaling events. Lipid rafts may also represent sites for the sequestered localization of certain membrane proteins. Among these are proteins with lipid modifications, such as glycosylphosphatidylinositol-anchored cell surface proteins and cytoplasmically oriented proteins with closely spaced myristoylation and palmitoylation, as well as other hydrophobic integral membrane proteins such as caveolin and flotillin (Baumann, C. A. et al. (2000) Nature (London) 407:202-207).

[0037] An essential role in intracellular signaling pathways is filled by second messenger molecules, intermediaries that are activated upon binding of ligands to surface receptors and serve as activators of downstream effector molecules. The cyclic nucleotides, adenosine 3′,5′-cyclic monophosphate (cAMP) and guanosine 3′5′-cyclic monophosphate (cGMP) are critical second messengers in a wide variety of signaling pathways. cAMP and cGMP are generated by the enzymes adenylyl (adenylate) cyclase (AC) and guanylyl (guanylate) cyclase (GC) from ATP and GTP. Thus a key step in regulating intracellular cAMP and cGMP levels is modulation of AC and GC activity.

[0038] Nogo has been identified as a component of the central nervous system myelin that prevents axonal regeneration in adult vertebrates. Cleavage of the Nogo-66 receptor and other glycophosphatidylinositol-linked proteins from axonal surfaces renders neurons insensitive to Nogo-66, facilitating potential recovery from CNS damage (Fournier, A. B. et al (2001) Nature 409:341-346).

[0039] The slit proteins are extracellular matrix proteins expressed by cells at the ventral midline of the nervous system. Slit proteins are ligands for the repulsive guidance receptor Roundabout (Robo) and thus play a role in repulsive axon guidance (Brose, K et al. (1999) Cell 96:795-806).

[0040] Lysosomes are the site of degradation of intracellular material during autophagy and of extracellular molecules following endocytosis. Lysosomal enzymes are packaged into vesicles which bud from the trans-Golgi network. These vesicles fuse with endosomes to form the mature lysosome in which hydrolytic digestion of endocytosed material occurs. Lysosomes can fuse with autophagosomes to form a unique compartment in which the degradation of organelles and other intracellular components occurs.

[0041] Protein sorting by transport vesicles, such as the endosome, has important consequences for a variety of physiological processes including cell surface growth, the biogenesis of distinct intracellular organelles, endocytosis, and the controlled secretion of hormones and neurotransmitters (Rothman, J. E. and Wieland, F. T. (1996) Science 272:227-234). In particular, neurodegenerative disorders and other neuronal pathologies are associated with biochemical flaws during endosomal protein sorting or endosomal biogenesis (Mayer R. J. et al. (1996) Adv. Exp. Med. Biol. 389:261-269).

[0042] Peroxisomes are organelles independent from the secretory pathway. They are the site of many peroxide-generating oxidative reactions in the cell. Peroxisomes are unique among eukaryotic organelles in that their size, number, and enzyme content vary depending upon organism, cell type, and metabolic needs (Waterham, H. R. and Cregg, J. M. (1997) BioEssays 19:57-66). Genetic defects in peroxisome proteins which result in peroxisomal deficiencies have been linked to a number of human pathologies, including Zellweger syndrome, rhizomelic chonrodysplasia punctata, X-linked adrenoleukodystrophy, acyl-CoA oxidase deficiency, bifunctional enzyme deficiency, classical Refsum's disease, DHAP alkyl transferase deficiency, and acatalasemia (Moser, H. W. and Moser, A. B. (1996) Ann. NY Acad. Sci. 804:427-441). In addition, Gartner, J. et al. (1991; Pediatr. Res. 29:141-146) found a 22 kDa integral membrane protein associated with lower density peroxisome-like subcellular fractions in patients with Zellweger syndrome.

[0043] Normal embryonic development and control of germ cell maturation is modulated by a number of secretory proteins which interact with their respective membrane-bound receptors. Cell fate during embryonic development is determined by members of the activin/TGF-β superfamily, cadherins, IGP-2, and other morphogens. In addition, proliferation, maturation, and redifferentiation of germ cell and reproductive tissues are regulated, for example, by IGF-2, inhibins, activins, and follistatins (Petraglia, F. (1997) Placenta 18:3-8; Mather, J. P. et al. (1997) Proc. Soc. Exp. Biol. Med. 215:209-222). Transforming growth factor beta (TGFbeta) signal transduction is mediated by two receptor Ser/Thr kinases acting in series, type II TGFbeta receptor and (TbetaRI-I) phosphorylating type I TGFbeta receptor (TbetaR-I). TbetaR-I-associated protein-1 (TRECAP-1), which distinguishes between quiescent and activated forms of the type I transforming growth factor beta receptor, has been associated with TGFbeta signaling (Charng, M. J et al. (1998) J. Biol. Chem. 273:9365-9368).

[0044] Retinoic acid receptor alpha (RAR alpha) mediates retinoic-acid induced maturation and has been implicated in myeloid development. Genes induced by retinoic acid during granulocytic differentiation include E3, a hematopoietic-specific gene that is an immediate target for the activated RAR alpha during myelopoiesis (Scott, L. M. et al. (1996) Blood 88:2517-2530).

[0045] The μ-opioid receptor (MOR) mediates the actions of analgesic agents including morphine, codeine, methadone, and fentanyl as well as heroin. MOR is functionally coupled to a G-protein-activated potassium channel (Mestek A. et al. (1995) 3. Neurosci. 15:2396-2406). A variety of MOR subtypes exist. Alternative splicing has been observed with MOR-1 as with a number of G protein-coupled receptors including somatostatin 2, dopamine D2, prostaglandin EP3, and serotonin receptor subtypes 5-hydroxytryptamnine4 and 5-hydroxytryptamine7 (Pan, Y. X. et al. (1999) Mol. Pharm 56:396-403).

[0046] Peripheral and Anchored Membrane Proteins

[0047] Some membrane proteins are not membrane-spanning but are attached to the plasma membrane via membrane anchors or interactions with integral membrane proteins. Membrane anchors are covalently joined to a protein post-translationally and include such moieties as prenyl, myristyl, and glycosylphosphatidyl inositol groups. Membrane localization of peripheral and anchored proteins is important for their function in processes such as receptor-mediated signal transduction. For example, prenylation of Ras is required for its localization to the plasma membrane and for its normal and oncogenic functions in signal transduction.

[0048] Synaptobrevins are synaptic vesicle-associated membrane proteins (VAMPs) which were first discovered in rat brain. These proteins were initially thought to be limited to neuronal cells and to function in the movement of vesicles from the plasmalemma of one cell, across the synapse, to the plasmalemma of another cell. Synaptobrevins are now known to occur and function in constitutive vesicle trafficking pathways involving receptor-mediated endocytotic and exocytotic pathways of many non-neuronal cell types. This regulated vesicle trafficking pathway may be blocked by the highly specific action of clostridial neurotoxins which cleave the synaptobrevin molecule.

[0049] In vitro studies of various cellular membranes (Galli et al (1994) J Cell Biol 125:1015-24; Link et al (1993) J Biol Chem 268:18423-6) have shown that VAMPS are widely distributed. These important membrane trafficking proteins appear to participate in axon extension via exocytosis during development, in the release of neurotransmitters and modulatory peptides, and in endocytosis. Endocytotic vesicular transport includes such intracellular events as the fusions and fissions of the nuclear membrane, endoplasmic reticulum, Golgi apparatus, and various inclusion bodies such as peroxisomes or lysosomes. Endocytotic processes appear to be universal in eukaryotic cells as diverse as yeast, Caenorhabditis elegans, Drosophila, and mammals.

[0050] VAMP-1B is involved in subcellular targeting and is an isoform of VAMP-1A (Isenmann, S. et al., (1998) Mol. Biol. Cell 9:1649-1660). Four additional splice variants (VAMP-1C to F) have recently been identified. Each variant has variable sequences only at the extreme C-terminus, suggesting that the C-terminus is important in vesicle targeting (Berglund, L. et al., (1999) Biochem. Biophys. Res. Commun. 264:777-780).

[0051] Lysosomes are the site of degradation of intracellular material during autophagy, and of extracellular molecules following endocytosis. Lysosomal enzymes are packaged into vesicles which bud from the trans-Golgi network. These vesicles fuse with endosomes to form the mature lysosome in which hydrolytic digestion of endocytosed material occurs. Lysosomes can fuse with autophagosomes to form a unique compartment in which the degradation of organelles and other intracellular components occurs.

[0052] Protein sorting by transport vesicles, such as the endosome, has important consequences for a variety of physiological processes including cell surface growth, the biogenesis of distinct intracellular organelles, endocytosis, and the controlled secretion of hormones and neurotransmitters (Rothman, J. E. and Wieland, F. T. (1996) Science 272:227-234). In particular, neurodegenerative disorders and other neuronal pathologies are associated with biochemical flaws during endosomal protein sorting or endosomal biogenesis (Mayer R. J. et al. (1996) Adv. Exp. Med. Biol. 389:261-269).

[0053] Peroxisomes are organelles independent from the secretory pathway. They are the site of many peroxide-generating oxidative reactions in the cell. Peroxisomes are unique among eukaryotic organelles in that their size, number, and enzyme content vary depending upon organism, cell type, and metabolic needs (Waterham, H. R. and Cregg, J. M. (1997) BioEssays 19:57-66). Genetic defects in peroxisome proteins which result in peroxisomal deficiencies have been linked to a number of human pathologies, including Zellweger syndrome, rhizomelic chondrodysplasia punctata, X-linked adrenoleukodystrophy, acyl-CoA oxidase deficiency, bifunctional enzyme deficiency, classical Refsum's disease, DHAP alkyl transferase deficiency, and acatalasemia (Moser, H. W. and Moser, A. B. (1996) Ann. NY Acad. Sci. 804:427-441). In addition, Gartner, J. et al. (1991; Pediatr. Res. 29:141-146) found a 22 kDa integral membrane protein associated with lower density peroxisome-like subcellular fractions in patients with Zellweger syndrome.

[0054] Normal embryonic development and control of germ cell maturation is modulated by a number of secretory proteins which interact with their respective membrane-bound receptors. Cell fate during embryonic development is determined by members of the activin/TGF-β superfamily, cadherins, IGF-2, and other morphogens. In addition, proliferation, maturation, and redifferentiation of germ cell and reproductive tissues are regulated, for example, by IGF-2, inhibins, activins, and follistatins (Petraglia, F. (1997) Placenta 18:3-8; Mather, J. P. et al. (1997) Proc. Soc. Exp. Biol. Med. 215:209-222).

[0055] Endoplasmic Reticulum Membrane Proteins

[0056] The normal functioning of the eukaryotic cell requires that all newly synthesized proteins be correctly folded, modified, and delivered to specific intra- and extracellular sites. Newly synthesized membrane and secretory proteins enter a cellular sorting and distribution network during or immediately after synthesis and are routed to specific locations inside and outside of the cell. The initial compartment in this process is the endoplasmic reticulum (ER) where proteins undergo modifications such as glycosylation, disulfide bond formation, and oligomerization. The modified proteins are then transported through a series of membrane-bound compartments which include the various cisternae of the Golgi complex, where further carbohydrate modifications occur. Transport between compartments occurs by means of vesicle budding and fusion. Once within the secretory pathway, proteins do not have to cross a membrane to reach the cell surface.

[0057] Although the majority of proteins processed through the ER are transported out of the organelle, some are retained. The signal for retention in the ER in mammalian cells consists of the tetrapeptide sequence, KDEL, located at the carboxyl terminus of resident ER membrane proteins (Munro, S. (1986) Cell 46:291-300). Proteins containing this sequence leave the ER but are quickly retrieved from the early Golgi cisternae and returned to the ER, while proteins lacking this signal continue through the secretory pathway.

[0058] Disruptions in the cellular secretory pathway have been implicated in several human diseases. In familial hypercholesterolemia the low density lipoprotein receptors remain in the ER, rather than moving to the cell surface (Pathak, R. K. (1988) J. Cell Biol. 106:1831-1841). Altered transport and processing of the β-amyloid precursor protein (βAPP) involves the putative vesicle transport protein presenilin and may play a role in early-onset Alzheimer's disease (Levy-Lahad, E. et al (1995) Science 269:973-977). Changes in ER-derived calcium homeostasis have been associated with diseases such as cardiomyopathy, cardiac hypertrophy, myotonic dystrophy, Brody disease, Smith-McCort dysplasia, and diabetes melitus.

[0059] Mitochondrial Membrane Proteins

[0060] The mitochondrial electron transport (or respiratory) chain is a series of three enzyme complexes in the mitochondrial membrane that is responsible for the transport of electrons from NADH to oxygen and the coupling of this oxidation to the synthesis of ATP (oxidative phosphorylation). ATP then provides the primary source of energy for driving the many energy-requiring reactions of a cell.

[0061] Most of the protein components of the mitochondrial respiratory chain are the products of nuclear encoded genes that are imported into the mitochondria, and the remainder are products of mitochondrial genes. Defects and altered expression of enzymes in the respiratory chain are associated with a variety of disease conditions in man, including, for example, neurodegenerative diseases, myopathies, and cancer.

[0062] Lymphocyte and Leukocyte Membrane Proteins

[0063] The B-cell response to antigens is an essential component of the normal immune system. Mature B cells recognize foreign antigens through B cell receptors (BCR) which are membrane-bound, specific antibodies that bind foreign antigens. The antigen/receptor complex is internalized, and the antigen is proteolytically processed. To generate an efficient response to complex antigens, the BCR, BCR-associated proteins, and T cell response are all required. Proteolytic fragments of the antigen are complexed with major histocompatability complex-II (MHCII) molecules on the surface of the B cells where the complex can be recognized by T cells. In contrast, macrophages and other lymphoid cells present antigens in association with MHCI molecules to T cells. T cells recognize and are activated by the MHCI-antigen complex through interactions with the T cell receptor/CD3 complex, a T cell-surface multimeric protein located in the plasma membrane. T cells activated by antigen presentation secrete a variety of lymphokines that induce B cell maturation and T cell proliferation, and activate macrophages, which kill target cells.

[0064] Leukocytes have a fundamental role in the inflammatory and immune response, and include monocytes/macrophages, mast cells, polymorphonucleoleukocytes, natural killer cells, neutrophils, eosinophils, basopbils, and myeloid precursors. Leukocyte membrane proteins include members of the CD antigens, N-CAM, I-CAM, human leukocyte antigen (HLA) class I and HLA class II gene products, immunoglobulins, immunoglobulin receptors, complement, complement receptors, interferons, interferon receptors, interleukin receptors, and chemokine receptors.

[0065] Abnormal lymphocyte and leukocyte activity has been associated with acute disorders such as AIDS, immune hypersensitivity, leukemias, leukopenia, systemic lupus, granulomatous disease, and eosinophilia.

[0066] Apoptosis-Associated Membrane Proteins

[0067] A variety of ligands, receptors, enzymes, tumor suppressors, viral gene products, pharmacological agents, and inorganic ions have important positive or negative roles in regulating and implementing the apoptotic destruction of a cell. Although some specific components of the apoptotic pathway have been identified and characterized, many interactions between the proteins involved are undefined, leaving major aspects of the pathway unknown.

[0068] A requirement for calcium in apoptosis was previously suggested by studies showing the involvement of calcium levels in DNA cleavage and Fas-mediated cell death (Hewish, D. R. and L. A. Burgoyne (1973) Biochem. Biophys. Res. Comm. 52:504-510; Vignaux, P. et al. (1995) J. Exp. Med. 181:781-386; Oshimi, Y. and S. Miyazaki (1995) J. Immunol. 154:599-609). Other studies show that intracellular calcium concentrations increase when apoptosis is triggered in thymocytes by either T cell receptor cross-linking or by glucocorticoids, and cell death can be prevented by blocking this increase (McConkey, D. J. et al. (1989) J. Immunol. 143:1801-1806; McConkey, D. J. et al. (1989) Arch. Biochem. Biophys. 269:365-370). Therefore, membrane proteins such as calcium channels and the Fas receptor are important for the apopoptic response.

[0069] Expression Profiling

[0070] Array technology can provide a simple way to explore the expression of a single polymorphic gene or the expression profile of a large number of related or unrelated genes. When the expression of a single gene is examined, arrays are employed to detect the expression of a specific gene or its variants. When an expression profile is examined, arrays provide a platform for identifying genes that are tissue specific, are affected by a substance being tested in a toxicology assay, are part of a signaling cascade, carry out housekeeping functions, or are specifically related to a particular genetic predisposition, condition, disease, or disorder.

[0071] The discovery of new receptors and membrane-associated proteins, and the polynucleotides encoding them, satisfies a need in the art by providing new compositions which are useful in the diagnosis, prevention, and treatment of cardiovascular, neurological, gastrointestinal, lipid metabolism, cell proliferative, autoimmune/inflammatory, metabolic, developmental, and endocrine disorders, and in the assessment of the effects of exogenous compounds on the expression of nucleic acid and amino acid sequences of receptors and membrane-associated proteins.

SUMMARY OF THE INVENTION

[0072] The invention features purified polypeptides, receptors and membrane-associated proteins, referred to collectively as “REMAP” and individually as “REMAP-1,” “REMAP-2,” “REMAP-3,” “REMAP-4,” “REMAP-5,” “REMAP-6,” “REMAP-7,” “REMAP-8,” “REMAP-9,” “REMAP-10,” “REMAP-11,” “REMAP-12,” “REMAP-13,” “REMAP-14,” “REMAP-15,” “REMAP-16,” “REMAP-17,” “REMAP-18,” “REMAP-19,” “REMAP-20,” “REMAP-21,” “REMAP-22,” “REMAP-23,” “REMAP-24,” “REMAP-25,” “REMAP-26,” “REMAP-27,” “REMAP-28,” “REMAP-29” “REMAP-30,” “REMAP-31,” “REMAP-32,” “REMAP-33,” “REMAP-34,” “REMAP-35,” “REMAP-36,” “REMAP-37,” “REMAP-38,” “REMAP-39,” “REMAP-40,” “REMAP-41,” “REMAP-42,” and “REMAP-43.” In one aspect, the invention provides an isolated polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. In one alternative, the invention provides an isolated polypeptide comprising the amino acid sequence of SEQ ID NO:1-43.

[0073] The invention further provides an isolated polynucleotide encoding a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. In one alternative, the polynucleotide encodes a polypeptide selected from the group consisting of SEQ ID NO:1-43. In another alternative, the polynucleotide is selected from the group consisting of SEQ ID NO:44-86.

[0074] Additionally, the invention provides a recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide encoding a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. In one alternative, the invention provides a cell transformed with the recombinant polynucleotide. In another alternative, the invention provides a transgenic organism comprising the recombinant polynucleotide.

[0075] The invention also provides a method for producing a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ D NO:1-43. The method comprises a) culturing a cell under conditions suitable for expression of the polypeptide, wherein said cell is transformed with a recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide encoding the polypeptide, and b) recovering the polypeptide so expressed.

[0076] Additionally, the invention provides an isolated antibody which specifically binds to a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.

[0077] The invention further provides an isolated polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). In one alternative, the polynucleotide comprises at least 60 contiguous nucleotides.

[0078] Additionally, the invention provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). The method comprises a) hybridizing the sample with a probe comprising at least 20 contiguous nucleotides comprising a sequence complementary to said target polynucleotide in the sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide or fragments thereof, and b) detecting the presence or absence of said hybridization complex, and optionally, if present, the amount thereof. In one alternative, the probe comprises at least 60 contiguous nucleotides.

[0079] The invention further provides a method for detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, c) a polynucleotide complementary to the polynucleotide of a), d) a polynucleotide complementary to the polynucleotide of b), and e) an RNA equivalent of a)-d). The method comprises a) amplify said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.

[0080] The invention further provides a composition comprising an effective amount of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and a pharmaceutically acceptable excipient. In one embodiment, the composition comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43. The invention additionally provides a method of treating a disease or condition associated with decreased expression of functional REMAP, comprising administering to a patient in need of such treatment the composition.

[0081] The invention also provides a method for screening a compound for effectiveness as an agonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting agonist activity in the sample. In one alternative, the invention provides a composition comprising an agonist compound identified by the method and a pharmaceutically acceptable excipient. In another alternative, the invention provides a method of treating a disease or condition associated with decreased expression of functional REMAP, comprising administering to a patient in need of such treatment the composition.

[0082] Additionally, the invention provides a method for screening a compound for effectiveness as an antagonist of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. The method comprises a) exposing a sample comprising the polypeptide to a compound, and b) detecting antagonist activity in the sample. In one alternative, the invention provides a composition comprising an antagonist compound identified by the method and a pharmaceutically acceptable excipient. In another alternative, the invention provides a method of treating a disease or condition associated with overexpression of functional REMAP, comprising administering to a patient in need of such treatment the composition.

[0083] The invention further provides a method of screening for a compound that specifically binds to a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ED NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. The method comprises a) combining the polypeptide with at least one test compound under suitable conditions, and b) detecting binding of the polypeptide to the test compound, thereby identifying a compound that specifically binds to the polypeptide.

[0084] The invention further provides a method of screening for a compound that modulates the activity of a polypeptide selected from the group consisting of a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, c) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and d) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43. The method comprises a) combining the polypeptide with at least one test compound under conditions permissive for the activity of the polypeptide, b) assessing the activity of the polypeptide in the presence of the test compound, and c) comparing the activity of the polypeptide in the presence of the test compound with the activity of the polypeptide in the absence of the test compound, wherein a change in the activity of the polypeptide in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide.

[0085] The invention further provides a method for screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, the method comprising a) exposing a sample comprising the target polynucleotide to a compound, b) detecting altered expression of the target polynucleotide, and c) comparing the expression of the target polynucleotide in the presence of varying amounts of the compound and in the absence of the compound.

[0086] The invention further provides a method for assessing toxicity of a test compound, said method comprising a) treating a biological sample containing nucleic acids with the test compound; b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, ii) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, iii) a polynucleotide having a sequence complementary to i), iv) a polynucleotide complementary to the polynucleotide of ii), and v) an RNA equivalent of i)-iv). Hybridization occurs under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide selected from the group consisting of i) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, ii) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, iii) a polynucleotide complementary to the polynucleotide of i), iv) a polynucleotide complementary to the polynucleotide of ii), and v) an RNA equivalent of i)-iv). Alternatively, the target polynucleotide comprises a fragment of a polynucleotide sequence selected from the group consisting of i)-v) above; c) quantify the amount of hybridization complex; and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the treated biological sample is indicative of toxicity of the test compound.

BRIEF DESCRIPTION OF THE TABLES

[0087] Table 1 summarizes the nomenclature for the full length polynucleotide and polypeptide sequences of the present invention.

[0088] Table 2 shows the GenBank identification number and annotation of the nearest GenBank homolog, for polypeptides of the invention. The probability scores for the matches between each polypeptide and its homolog(s) are also shown.

[0089] Table 3 shows structural features of polypeptide sequences of the invention, including predicted motifs and domains, along with the methods, algorithms, and searchable databases used for analysis of the polypeptides.

[0090] Table 4 lists the cDNA and/or genomic DNA fragments which were used to assemble polynucleotide sequences of the invention, along with selected fragments of the polynucleotide sequences.

[0091] Table 5 shows the representative cDNA library for polynucleotides of the invention.

[0092] Table 6 provides an appendix which describes the tissues and vectors used for construction of the cDNA libraries shown in Table 5.

[0093] Table 7 shows the tools, programs, and algorithms used to analyze the polynucleotides and polypeptides of the invention, along with applicable descriptions, references, and threshold parameters.

DESCRIPTION OF THE INVENTION

[0094] Before the present proteins, nucleotide sequences, and methods are described, it is understood that this invention is not limited to the particular machines, materials and methods described, as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims.

[0095] It must be noted that as used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to “a host cell” includes a plurality of such host cells, and a reference to “an antibody” is a reference to one or more antibodies and equivalents thereof known to those skilled in the art, and so forth.

[0096] Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any machines, materials, and methods similar or equivalent to those described herein can be used to practice or test the present invention, the preferred machines, materials and methods are now described. All publications mentioned herein are cited for the purpose of describing and disclosing the cell lines, protocols, reagents and vectors which are reported in the publications and which might be used in connection with the invention. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention.

[0097] Definitions

[0098] “REMAP” refers to the amino acid sequences of substantially purified REMAP obtained from any species, particularly a mammalian species, including bovine, ovine, porcine, murine, equine, and human, and from any source, whether natural, synthetic, semi-synthetic, or recombinant.

[0099] The term “agonist” refers to a molecule which intensifies or mimics the biological activity of REMAP. Agonists may include proteins, nucleic acids, carbohydrates, small molecules, or any other compound or composition which modulates the activity of REMAP either by directly interacting with REMAP or by acting on components of the biological pathway in which REMAP participates.

[0100] An “allelic variant” is an alternative form of the gene encoding REMAP. Allelic variants may result from at least one mutation in the nucleic acid sequence and may result in altered mRNAs or in polypeptides whose structure or function may or may not be altered. A gene may have none, one, or many allelic variants of its naturally occurring form. Common mutational changes which give rise to allelic variants are generally ascribed to natural deletions, additions, or substitutions of nucleotides. Each of these types of changes may occur alone, or in combination with the others, one or more times in a given sequence.

[0101] “Altered” nucleic acid sequences encoding REMAP include those sequences with deletions, insertions, or substitutions of different nucleotides, resulting in a polypeptide the same as REMAP or a polypeptide with at least one functional characteristic of REMAP. Included within this definition are polymorphisms which may or may not be readily detectable using a particular oligonucleotide probe of the polynucleotide encoding REMAP, and improper or unexpected hybridization to allelic variants, with a locus other than the normal chromosomal locus for the polynucleotide sequence encoding REMAP. The encoded protein may also be “altered,” and may contain deletions, insertions, or substitutions of amino acid residues which produce a silent change and result in a functionally equivalent REMAP. Deliberate amino acid substitutions may be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity, and/or the amphipathic nature of the residues, as long as the biological or immunological activity of REMAP is retained. For example, negatively charged amino acids may include aspartic acid and glutamic acid, and positively charged amino acids may include lysine and arginine. Amino acids with uncharged polar side chains having similar hydrophilicity values may include: asparagine and glutamine; and serine and threonine. Amino acids with uncharged side chains having similar hydrophilicity values may include: leucine, isoleucine, and valine; glycine and alanine; and phenylalanine and tyrosine.

[0102] The terms “amino acid” and “amino acid sequence” refer to an oligopeptide, peptide, polypeptide, or protein sequence, or a fragment of any of these, and to naturally occurring or synthetic molecules. Where “amino acid sequence” is recited to refer to a sequence of a naturally occurring protein molecule, “amino acid sequence” and like terms are not meant to limit the amino acid sequence to the complete native amino acid sequence associated with the recited protein molecule.

[0103] “Amplification” relates to the production of additional copies of a nucleic acid sequence. Amplification is generally carried out using polymerase chain reaction PCR) technologies well known in the art.

[0104] The term “antagonist” refers to a molecule which inhibits or attenuates the biological activity of REMAP. Antagonists may include proteins such as antibodies, nucleic acids, carbohydrates, small molecules, or any other compound or composition which modulates the activity of REMAP either by directly interacting with REMAP or by acting on components of the biological pathway in which REMAP participates.

[0105] The term “antibody” refers to intact immunoglobulin molecules as well as to fragments thereof, such as Fab, F(ab′)₂, and Fv fragments, which are capable of binding an epitopic determinant. Antibodies that bind REMAP polypeptides can be prepared using intact polypeptides or using fragments containing small peptides of interest as the immunizing antigen. The polypeptide or oligopeptide used to immunize an animal (e.g., a mouse, a rat, or a rabbit) can be derived from the translation of RNA, or synthesized chemically, and can be conjugated to a carrier protein if desired. Commonly used carriers that are chemically coupled to peptides include bovine serum albumin, thyroglobulin, and keyhole limpet hemocyanin (KLH). The coupled peptide is then used to immunize the animal.

[0106] The term “antigenic determinant” refers to that region of a molecule (i.e., an epitope) that makes contact with a particular antibody. When a protein or a fragment of a protein is used to immunize a host animal, numerous regions of the protein may induce the production of antibodies which bind specifically to antigenic determinants (particular regions or three-dimensional structures on the protein). An antigenic determinant may compete with the intact antigen (i.e., the immunogen used to elicit the immune response) for binding to an antibody.

[0107] The term “aptamer” refers to a nucleic acid or oligonucleotide molecule that binds to a specific molecular target. Aptamers are derived from an in vitro evolutionary process (e.g., SELUX (Systematic Evolution of Ligands by EXponential Enrichment), described in U.S. Pat. No. 5,270,163), which selects for target-specific aptamer sequences from large combinatorial libraries. Aptamer compositions maybe double-stranded or single-stranded, and may include deoxynbonucleotides, ribonucleotides, nucleotide derivatives, or other nucleotide-like molecules. The nucleotide components of an aptamer may have modified sugar groups (e.g., the 2′-OH group of a ribonucleotide may be replaced by 2′-F or 2′-NH₂), which may improve a desired property, e.g., resistance to nucleases or longer lifetime in blood. Aptamers may be conjugated to other molecules, e.g., a high molecular weight carrier to slow clearance of the aptamer from the circulatory system. Aptamers may be specifically cross-linked to their cognate ligands, e.g., by photo-activation of a cross-linker. (See, e.g., Brody, E. N. and L. Gold (2000) J. Biotechnol. 74:5-13.)

[0108] The term “intramer” refers to an aptamer which is expressed in vivo. For example, a vaccinia virus-based RNA expression system has been used to express specific RNA aptamers at high levels in the cytoplasm of leukocytes (Blind, M. et al. (1999) Proc. Natl Acad. Sci. USA 96:3606-3610).

[0109] The term “spiegelmer” refers to an aptamer which includes L-DNA, L-RNA, or other left-handed nucleotide derivatives or nucleotide-like molecules. Aptamers containing left-handed nucleotides are resistant to degradation by naturally occurring enzymes, which normally act on substrates containing right-handed nucleotides.

[0110] The term “antisense” refers to any composition capable of base-pairing with the “sense” (coding) strand of a specific nucleic acid sequence. Antisense compositions may include DNA; RNA; peptide nucleic acid (PNA); oligonucleotides having modified backbone linkages such as phosphorothioates, methylphosphonates, or benzylphosphonates; oligonucleotides having modified sugar groups such as 2′-methoxyethyl sugars or 2′-methoxyethoxy sugars; or oligonucleotides having modified bases such as 5-methyl cytosine, 2′-deoxyiracil, or 7-deaza-2′-deoxyguanosine. Antisense molecules may be produced by any method including chemical synthesis or transcription. Once introduced into a cell, the complementary antisense molecule base-pairs with a naturally occurring nucleic acid sequence produced by the cell to form duplexes which block either transcription or translation. The designation “negative” or “minus” can refer to the antisense strand, and the designation “positive” or “plus” can refer to the sense strand of a reference DNA molecule.

[0111] The term “biologically active” refers to a protein having structural, regulatory, or biochemical functions of a naturally occurring molecule. Likewise, “immunologically active” or “immunogenic” refers to the capability of the natural, recombinant, or synthetic REMAP, or of any oligopeptide thereof, to induce a specific immune response in appropriate animals or cells and to bind with specific antibodies.

[0112] “Complementary” describes the relationship between two single-stranded nucleic acid sequences that anneal by base-pairing. For example, 5′-AGT-3′ pairs with its complement, 3′-TCA-5′.

[0113] A “composition comprising a given polynucleotide sequence” and a “composition comprising a given amino acid sequence” refer broadly to any composition containing the given polynucleotide or amino acid sequence. The composition may comprise a dry formulation or an aqueous solution. Compositions comprising polynucleotide sequences encoding REMAP or fragments of REMAP may be employed as hybridization probes. The probes may be stored in freeze-dried form and may be associated with a stabilizing agent such as a carbohydrate. In hybridizations, the probe may be deployed in an aqueous solution containing salts (e.g., NaCl), detergents (e.g., sodium dodecyl sulfate; SDS), and other components (e.g., Denhardt's solution, dry milk, salmon sperm DNA, etc.).

[0114] “Consensus sequence” refers to a nucleic acid sequence which has been subjected to repeated DNA sequence analysis to resolve uncalled bases, extended using the XL-PCR kit (Applied Biosystems, Foster City Calif.) in the 5′ and/or the 3′ direction, and resequenced, or which has been assembled from one or more overlapping cDNA, EST, or genomic DNA fragments using a computer program for fragment assembly, such as the GELVIEW fragment assembly system (GCG, Madison Wis.) or Phrap (University of Washington, Seattle Wash.). Some sequences have been both extended and assembled to produce the consensus sequence.

[0115] “Conservative amino acid substitutions” are those substitutions that are predicted to least interfere with the properties of the original protein, i.e., the structure and especially the function of the protein is conserved and not significantly changed by such substitutions. The table below shows amino acids which maybe substituted for an original amino acid in a protein and which are regarded as conservative amino acid substitutions. Original Residue Conservative Substitution Ala Gly, Ser Arg His, Lys Asn Asp, Gln, His Asp Asn, Glu Cys Ala, Ser Gln Asn, Glu, His Glu Asp, Gln, His Gly Ala His Asn, Arg, Gln, Glu Ile Leu, Val Leu Ile, Val Lys Arg, Gln, Glu Met Leu, Ile Phe His, Met, Leu, Trp, Tyr Ser Cys, Thr Thr Ser, Val Trp Phe, Tyr Tyr His, Phe, Trp Val Ile, Leu, Thr

[0116] Conservative amino acid substitutions generally maintain (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a beta sheet or alpha helical conformation, (b) the charge or hydrophobicity of the molecule at the site of the substitution, and/or (c) the bulk of the side chain.

[0117] A “deletion” refers to a change in the amino acid or nucleotide sequence that results in the absence of one or more amino acid residues or nucleotides.

[0118] The term “derivative” refers to a chemically modified polynucleotide or polypeptide. Chemical modifications of a polynucleotide can include, for example, replacement of hydrogen by an alkyl, acyl, hydroxyl, or amino group. A derivative polynucleotide encodes a polypeptide which retains at least one biological or immunological function of the natural molecule. A derivative polypeptide is one modified by glycosylation, pegylation, or any similar process that retains at least one biological or immunological function of the polypeptide from which it was derived.

[0119] A “detectable label” refers to a reporter molecule or enzyme that is capable of generating a measurable signal and is covalently or noncovalently joined to a polynucleotide or polypeptide.

[0120] “Differential expression” refers to increased or upregulated; or decreased, downregulated, or absent gene or protein expression, determined by comparing at least two different samples. Such comparisons may be carried out between, for example, a treated and an untreated sample, or a diseased and a normal sample.

[0121] “Exon shuffling” refers to the recombination of different coding regions (exons). Since an exon may represent a structural or functional domain of the encoded protein, new proteins may be assembled through the novel reassortment of stable substructures, thus allowing acceleration of the evolution of new protein functions.

[0122] A “fragment” is a unique portion of REMAP or the polynucleotide encoding REMAP which is identical in sequence to but shorter in length than the parent sequence. A fragment may comprise up to the entire length of the defined sequence, minus one nucleotide/amino acid residue. For example, a fragment may comprise from 5 to 1000 contiguous nucleotides or amino acid residues. A fragment used as a probe, primer, antigen, therapeutic molecule, or for other purposes, maybe at least 5, 10, 15, 16, 20, 25, 30, 40, 50, 60, 75, 100, 150, 250 or at least 500 contiguous nucleotides or amino acid residues in length. Fragments may be preferentially selected from certain regions of a molecule. For example, a polypeptide fragment may comprise a certain length of contiguous amino acids selected from the first 250 or 500 amino acids (or first 25% or 50%) of a polypeptide as shown in a certain defined sequence. Clearly these lengths are exemplary, and any length that is supported by the specification, including the Sequence Listing, tables, and figures, may be encompassed by the present embodiments.

[0123] A fragment of SEQ ID NO:44-86 comprises a region of unique polynucleotide sequence that specifically identifies SEQ ID NO:44-86, for example, as distinct from any other sequence in the genome from which the fragment was obtained. A fragment of SEQ ID NO:44-86 is useful, for example, in hybridization and amplification technologies and in analogous methods that distinguish SEQ ID NO:44-86 from related polynucleotide sequences. The precise length of a fragment of SEQ ID NO:44-86 and the region of SEQ ID NO:44-86 to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment.

[0124] A fragment of SEQ ID NO:1-43 is encoded by a fragment of SEQ ID NO:44-86. A fragment of SEQ ID NO:1-43 comprises a region of unique amino acid sequence that specifically identifies SEQ ID NO:1-43. For example, a fragment of SEQ ID NO:1-43 is useful as an immunogenic peptide for the development of antibodies that specifically recognize SEQ ID NO: 1-43. The precise length of a fragment of SEQ ID NO:1-43 and the region of SEQ ID NO:1-43 to which the fragment corresponds are routinely determinable by one of ordinary skill in the art based on the intended purpose for the fragment

[0125] A “full length” polynucleotide sequence is one containing at least a translation initiation codon (e.g., methionine) followed by an open reading frame and a translation termination codon. A “full length” polynucleotide sequence encodes a “full length” polypeptide sequence.

[0126] “Homology” refers to sequence similarity or, interchangeably, sequence identity, between two or more polynucleotide sequences or two or more polypeptide sequences.

[0127] The terms “percent identity” and “% identity,” as applied to polynucleotide sequences, refer to the percentage of residue matches between at least two polynucleotide sequences aligned using a standardized algorithm. Such an algorithm may insert, in a standardized and reproducible way, gaps in the sequences being compared in order to optimize alignment between two sequences, and therefore achieve a more meaningful comparison of the two sequences.

[0128] Percent identity between polynucleotide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program This program is part of the LASERGENE software package, a suite of molecular biological analysis programs (DNASTAR, Madison Wis.). CLUSTAL V is described in Higgins, D. G. and P. M. Sharp (1989) CABIOS 5:151-153 and in Higgins, D. G. et al. (1992) CABIOS 8:189-191. For pairwise alignments of polynucleotide sequences, the default parameters are set as follows: Ktuple=2, gap penalty=5, window=4, and “diagonals saved”=4. The “weighted” residue weight table is selected as the default. Percent identity is reported by CLUSTAL V as the “percent, similarity” between aligned polynucleotide sequences.

[0129] Alternatively, a suite of commonly used and freely available sequence comparison algorithms is provided by the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) (Altschul, S. F. et al. (1990) J. Mol. Biol. 215:403-410), which is available from several sources, including the NCBI, Bethesda, Md., and on the Internet at http://www.ncbi.nlm.nih.gov/BLAST/. The BLAST software suite includes various sequence analysis programs including “blastn,” that is used to align a known polynucleotide sequence with other polynucleotide sequences from a variety of databases. Also available is a tool called “BLAST 2 Sequences” that is used for direct pairwise comparison of two nucleotide sequences. “BLAST 2 Sequences” can be accessed and used interactively at http://www.ncbi.nlm.nih.gov/gorf/b12.html. The “BLAST 2 Sequences” tool can be used for both blastn and blastp (discussed below). BLAST programs are commonly used with gap and other parameters set to default settings. For example, to compare two nucleotide sequences, one may use blasta with the “BLAST 2 Sequences” tool Version 2.0.12 (Apr. 21, 2000) set at default parameters. Such default parameters may be, for example:

[0130] Matrix: BLOSUM62

[0131] Reward for match: 1

[0132] Penalty for mismatch: −2

[0133] Open Gap: 5 and Extension Gap: 2 penalties

[0134] Gap x drop-off. 50

[0135] Expect: 10

[0136] Word Size: 11

[0137] Filter: on

[0138] Percent identity may be measured over the length of an entire defined sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined sequence, for instance, a fragment of at least 20, at least 30, at least 40, at least 50, at least 70, at least 100, or at least 200 contiguous nucleotides. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in the tables, figures, or Sequence Listing, maybe used to describe a length over which percentage identity may be measured.

[0139] Nucleic acid sequences that do not show a high degree of identity may nevertheless encode similar amino acid sequences due to the degeneracy of the genetic code. It is understood that changes in a nucleic acid sequence can be made using this degeneracy to produce multiple nucleic acid sequences that all encode substantially the same protein.

[0140] The phrases “percent identity” and “% identity,” as applied to polypeptide sequences, refer to the percentage of residue matches between at least two polypeptide sequences aligned using a standardized algorithm. Methods of polypeptide sequence alignment are well-known. Some alignment methods take into account conservative amino acid substitutions. Such conservative substitutions, explained in more detail above, generally preserve the charge and hydrophobicity at the site of substitution, thus preserving the structure (and therefore function) of the polypeptide.

[0141] Percent identity between polypeptide sequences may be determined using the default parameters of the CLUSTAL V algorithm as incorporated into the MEGALIGN version 3.12e sequence alignment program (described and referenced above). For pairwise alignments of polypeptide sequences using CLUSTAL V, the default parameters are set as follows: Ktuple=1, gap penalty=3, window=5, and “diagonals saved”=5. The PAM250 matrix is selected as the default residue weight table. As with polynucleotide alignments, the percent identity is reported by CLUSTAL V as the “percent similarity” between aligned polypeptide sequence pairs.

[0142] Alternatively the NCBI BLAST software suite may be used. For example, for a pairwise comparison of two polypeptide sequences, one may use the “BLAST 2 Sequences” tool Version 2.0.12 (Apr. 21, 2000) with blastp set at default parameters. Such default parameters may be, for example:

[0143] Matrix: BLOSUM62

[0144] Open Gap: 11 and Extension Gap: 1 penalties

[0145] Gap x drop-off: 50

[0146] Expect: 10

[0147] Word Size: 3

[0148] Filter: on

[0149] Percent identity may be measured over the length of an entire defined polypeptide sequence, for example, as defined by a particular SEQ ID number, or may be measured over a shorter length, for example, over the length of a fragment taken from a larger, defined polypeptide sequence, for instance, a fragment of at least 15, at least 20, at least 30, at least 40, at least 50, at least 70 or at least 150 contiguous residues. Such lengths are exemplary only, and it is understood that any fragment length supported by the sequences shown herein, in the tables, figures or Sequence Listing, may be used to describe a length over which percentage identity may be measured.

[0150] “Human artificial chromosomes” (HACS) are linear microchromosomes which may contain DNA sequences of about 6 kb to 10 Mb in size and which contain all of the elements required for chromosome replication, segregation and maintenance.

[0151] The term “humanized antibody” refers to an antibody molecule in which the amino acid sequence in the non-antigen binding regions has been altered so that the antibody more closely resembles a human antibody, and still retains its original binding ability.

[0152] “Hybridization” refers to the process by which a polynucleotide strand anneals with a complementary strand through base pairing under defined hybridization conditions. Specific hybridization is an indication that two nucleic acid sequences share a high degree of complementarity. Specific hybridization complexes form under permissive annealing conditions and remain hybridized after the “washing” step(s). The washing step(s) is particularly important in determining the stringency of the hybridization process, with more stringent conditions allowing less non-specific binding, i.e., binding between pairs of nucleic acid strands that are not perfectly matched. Permissive conditions for annealing of nucleic acid sequences are routinely determinable by one of ordinary skill in the art and may be consistent among hybridization experiments, whereas wash conditions may be varied among experiments to achieve the desired stringency, and therefore hybridization specificity. Permissive annealing conditions occur, for example, at 68° C in the presence of about 6× SSC, about 1% (w/v) SDS, and about 100 μg/ml sheared, denatured salmon sperm DNA.

[0153] Generally, stringency of hybridization is expressed, in part, with reference to the temperature under which the wash step is carried out. Such wash temperatures are typically selected to be about 5° C. to 20° C. lower than the thermal melting point (T_(m)) for the specific sequence at a defined ionic strength and pH. The T_(m) is the temperature (under defined ionic strength and pH) at which 50% of the target sequence hybridizes to a perfectly matched probe. An equation for calculating T_(m) and conditions for nucleic acid hybridization are well known and can be found in Sambrook, J. et al. (1989) Molecular Cloning: A Laboratory Manual, 2nd ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; specifically see volume 2, chapter 9.

[0154] High stringency conditions for hybridization between polynucleotides of the present invention include wash conditions of 68° C. in the presence of about 0.2× SSC and about 0.1% SDS, for 1 hour. Alternatively, temperatures of about 65° C., 60° C., 55° C., or 42° C. maybe used. SSC concentration may be varied from about 0.1 to 2× SSC, with SDS being present at about 0.1%. Typically, blocking reagents are used to block non-specific hybridization. Such blocking reagents include, for instance, sheared and denatured salmon sperm DNA at about 100-200 μg/ml. Organic solvent, such as formamide at a concentration of about 35-50% v/v, may also be used under particular circumstances, such as for RNA:DNA hybridizations. Useful variations on these wash conditions will be readily apparent to those of ordinary skill in the art. Hybridization, particularly under high stringency conditions, may be suggestive of evolutionary similarity between the nucleotides. Such similarity is strongly indicative of a similar role for the nucleotides and their encoded polypeptides.

[0155] The term “hybridization complex” refers to a complex formed between two nucleic acid sequences by virtue of the formation of hydrogen bonds between complementary bases. A hybridization complex may be formed in solution (e.g., C₀t or R₀t analysis) or formed between one nucleic acid sequence present in solution and another nucleic acid sequence immobilized on a solid support (e.g., paper, membranes, filters, chips, pins or glass slides, or any other appropriate substrate to which cells or their nucleic acids have been fixed).

[0156] The words “insertion” and “addition” refer to changes in an amino acid or nucleotide sequence resulting in the addition of one or more amino acid residues or nucleotides, respectively.

[0157] “Immune response” can refer to conditions associated with inflammation, trauma, immune disorders, or infectious or genetic disease, etc. These conditions can be characterized by expression of various factors, e.g., cytokines, chemokines, and other signaling molecules, which may affect cellular and systemic defense systems.

[0158] An “immunogenic fragment” is a polypeptide or oligopeptide fragment of RBMAP which is capable of eliciting an immune response when introduced into a living organism, for example, a mammal. The term “immunogenic fragment” also includes any polypeptide or oligopeptide fragment of REMAP which is useful in any of the antibody production methods disclosed herein or known in the art.

[0159] The term “microarray” refers to an arrangement of a plurality of polynucleotides, polypeptides, or other chemical compounds on a substrate.

[0160] The terms “element” and “array element” refer to a polynucleotide, polypeptide, or other chemical compound having a unique and defined position on a microarray.

[0161] The term “modulate” refers to a change in the activity of REMAP. For example, modulation may cause an increase or a decrease in protein activity, binding characteristics, or any other biological, functional, or immunological properties of REMAP.

[0162] The phrases “nucleic acid” and “nucleic acid sequence” refer to a nucleotide, oligonucleotide, polynucleotide, or any fragment thereof. These phrases also refer to DNA or RNA of genomic or synthetic origin which may be single-stranded or double-stranded and may represent the sense or the antisense strand, to peptide nucleic acid (PNA), or to any DNA-like or RNA-like material

[0163] “Operably linked” refers to the situation in which a first nucleic acid sequence is placed in a functional relationship with a second nucleic acid sequence. For instance, a promoter is operably linked to a coding sequence if the promoter affects the transcription or expression of the coding sequence. Operably linked DNA sequences may be in close proximity or contiguous and, where necessary to join two protein coding regions, in the same reading frame.

[0164] “Peptide nucleic acid” (PNA) refers to an antisense molecule or anti-gene agent which comprises an oligonucleotide of at least about 5 nucleotides in length linked to a peptide backbone of amino acid residues ending in lysine. The terminal lysine confers solubility to the composition. PNAs preferentially bind complementary single stranded DNA or RNA and stop transcript elongation, and may be pegylated to extend their lifespan in the cell.

[0165] “Post-translational modification” of an REMAP may involve lipidation, glycosylation, phosphorylation, acetylation, racemization, proteolytic cleavage, and other modifications known in the art. These processes may occur synthetically or biochemically. Biochemical modifications will vary by cell type depending on the enzymatic milieu of REMAP.

[0166] “Probe” refers to nucleic acid sequences encoding REMAP, their complements, or fragments thereof, which are used to detect identical, allelic or related nucleic acid sequences. Probes are isolated oligonucleotides or polynucleotides attached to a detectable label or reporter molecule. Typical labels include radioactive isotopes, ligands, chemiluminescent agents, and enzymes. “Primers” are short nucleic acids, usually DNA oligonucleotides, which maybe annealed to a target polynucleotide by complementary base-pairing. The primer may then be extended along the target DNA strand by a DNA polymerase enzyme. Primer pairs can be used for amplification (and identification) of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR).

[0167] Probes and primers as used in the present invention typically comprise at least 15 contiguous nucleotides of a known sequence. In order to enhance specificity, longer probes and primers may also be employed, such as probes and primers that comprise at least 20, 25, 30, 40, 50, 60, 70, 80, 90, 100, or at least 150 consecutive nucleotides of the disclosed nucleic acid sequences. Probes and primers may be considerably longer than these examples, and it is understood that any length supported by the specification, including the tables, figures, and Sequence Listing, may be used.

[0168] Methods for preparing and using probes and primers are described in the references, for example Sambrook, J. et al. (1989) Molecular Cloning: A Laboratory Manual, 2^(nd) ed., vol. 1-3, Cold Spring Harbor Press, Plainview N.Y.; Ausubel, F. M. et al. (1987) Current Protocols in Molecular Biology, Greene Publ. Assoc. & Wiley-Intersciences, New York N.Y.; Innis, M. et al. (1990) PCR Protocols, A Guide to Methods and Applications, Academic Press, San Diego Calif. PCR primer pairs can be derived from a known sequence, for example, by using computer programs intended for that purpose such as Primer (Version 0.5, 1991, Whitehead Institute for Biomedical Research, Cambridge Mass.).

[0169] Oligonucleotides for use as primers are selected using software known in the art for such purpose. For example, OLIGO 4.06 software is useful for the selection of PCR primer pairs of up to 100 nucleotides each, and for the analysis of oligonucleotides and larger polynucleotides of up to 5,000 nucleotides from an input polynucleotide sequence of up to 32 kilobases. Similar primer selection programs have incorporated additional features for expanded capabilities. For example, the PrimOU primer selection program (available to the public from the Genome Center at University of Texas South West Medical Center, Dallas Tex.) is capable of choosing specific primers from megabase sequences and is thus useful for designing primers on a genome-wide scope. The Primer3 primer selection program (available to the public from the Whitehead Institute/MIT Center for Genome Research, Cambridge Mass.) allows the user to input a “mispriming library,” in which sequences to avoid as primer binding sites are user-specified. Primer3 is useful, in particular, for the selection of oligonucleotides for microarrays. (The source code for the latter two primer selection programs may also be obtained from their respective sources and modified to meet the user's specific needs.) The PrimeGen program (available to the public from the UK Human Genome Mapping Project Resource Centre, Cambridge UK) designs primers based on multiple sequence alignments, thereby allowing selection of primers that hybridize to either the most conserved or least conserved regions of aligned nucleic acid sequences. Hence, this program is useful for identification of both unique and conserved oligonucleotides and polynucleotide fragments. The oligonucleotides and polynucleotide fragments identified by any of the above selection methods are useful in hybridization technologies, for example, as PCR or sequencing primers, microarray elements, or specific probes to identify fully or partially complementary polynucleotides in a sample of nucleic acids. Methods of oligonucleotide selection are not limited to those described above.

[0170] A “recombinant nucleic acid” is a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two or more otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques such as those described in Sambrook, supra. The term recombinant includes nucleic acids that have been altered solely by addition, substitution, or deletion of a portion of the nucleic acid. Frequently, a recombinant nucleic acid may include a nucleic acid sequence operably linked to a promoter sequence. Such a recombinant nucleic acid maybe part of a vector that is used, for example, to transform a cell.

[0171] Alternatively, such recombinant nucleic acids maybe part of a viral vector, e.g., based on a vaccinia virus, that could be use to vaccinate a mammal wherein the recombinant nucleic acid is expressed, inducing a protective immunological response in the mammal.

[0172] A “regulatory element” refers to a nucleic acid sequence usually derived from untranslated regions of a gene and includes enhancers, promoters, introns, and 5′ and 3′ untranslated regions (UTRs). Regulatory elements interact with host or viral proteins which control transcription, translation, or RNA stability.

[0173] “Reporter molecules” are chemical or biochemical moieties used for labeling a nucleic acid, amino acid, or antibody. Reporter molecules include radionuclides; enzymes; fluorescent, chemiluminescent, or chromogenic agents; substrates; cofactors; inhibitors; magnetic particles; and other moieties known in the art.

[0174] An “RNA equivalent,” in reference to a DNA sequence, is composed of the same linear sequence of nucleotides as the reference DNA sequence with the exception that all occurrences of the nitrogenous base thymine are replaced with uracil, and the sugar backbone is composed of ribose instead of deoxyribose.

[0175] The term “sample” is used in its broadest sense. A sample suspected of containing REMAP, nucleic acids encoding REMAP, or fragments thereof may comprise a bodily fluid; an extract from a cell, chromosome, organelle, or membrane isolated from a cell; a cell; genomic DNA, RNA, or cDNA, in solution or bound to a substrate; a tissue; a tissue print; etc.

[0176] The terms “specific binding” and “specifically binding” refer to that interaction between a protein or peptide and an agonist, an antibody, an antagonist, a small molecule, or any natural or synthetic binding composition. The interaction is dependent upon the presence of a particular structure of the protein, e.g., the antigenic determinant or epitope, recognized by the binding molecule. For example, if an antibody is specific for epitope “A,” the presence of a polypeptide comprising the epitope A, or the presence of free unlabeled A, in a reaction containing free labeled A and the antibody will reduce the amount of labeled A that binds to the antibody.

[0177] The term “substantially purified” refers to nucleic acid or amino acid sequences that are removed from their natural environment and are isolated or separated, and are at least 60% free, preferably at least 75% free, and most preferably at least 90% free from other components with which they are naturally associated.

[0178] A “substitution” refers to the replacement of one or more amino acid residues or nucleotides by different amino acid residues or nucleotides, respectively.

[0179] “Substrate” refers to any suitable rigid or semi-rigid support including membranes, filters, chips, slides, wafers, fibers, magnetic or nonmagnetic beads, gels, tubing, plates, polymers, microparticles and capillaries. The substrate can have a variety of surface forms, such as wells, trenches, pins, channels and pores, to which polynucleotides or polypeptides are bound.

[0180] A “transcript image” or “expression profile” refers to the collective pattern of gene expression by a particular cell type or tissue under given conditions at a given time.

[0181] “Transformation” describes a process by which exogenous DNA is introduced into a recipient cell. Transformation may occur under natural or artificial conditions according to various methods well known in the art, and may rely on any known method for the insertion of foreign nucleic acid sequences into a prokaryotic or eukaryotic host cell. The method for transformation is selected based on the type of host cell being transformed and may include, but is not limited to, bacteriophage or viral infection, electroporation, heat shock, lipofection, and particle bombardment. The term “transformed cells” includes stably transformed cells in which the inserted DNA is capable of replication either as an autonomously replicating plasmid or as part of the host chromosome, as well as transiently transformed cells which express the inserted DNA or RNA for limited periods of time.

[0182] A “transgenic organism,” as used herein, is any organism, including but not limited to animals and plants, in which one or more of the cells of the organism contains heterologous nucleic acid introduced by way of human intervention, such as by transgenic techniques well known in the art. The nucleic acid is introduced into the cell, directly or indirectly by introduction into a precursor of the cell, by way of deliberate genetic manipulation, such as by microinjection or by infection with a recombinant virus. The term genetic manipulation does not include classical cross-breeding, or in vitro fertilization, but rather is directed to the introduction of a recombinant DNA molecule. The transgenic organisms contemplated in accordance with the present invention include bacteria, cyanobacteria, fungi, plants and animals. The isolated DNA of the present invention can be introduced into the host by methods known in the art, for example infection, transfection, transformation or transconjugation. Techniques for transferring the DNA of the present invention into such organisms are widely known and provided in references such as Sambrook et al. (1989), supra.

[0183] A “variant” of a particular nucleic acid sequence is defined as a nucleic acid sequence having at least 40% sequence identity to the particular nucleic acid sequence over a certain length of one of the nucleic acid sequences using blastn with the “BLAST 2 Sequences” tool Version 2.0.9 (May 7, 1999) set at default parameters. Such a pair of nucleic acids may show, for example, at least 50%, at least 60%, at least 70%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length. A variant may be described as, for example, an “allelic” (as defined above), “splice,” “species,” or “polymorphic” variant. A splice variant may have significant identity to a reference molecule, but will generally have a greater or lesser number of polynucleotides due to alternate splicing of exons during mRNA processing. The corresponding polypeptide may possess additional functional domains or lack domains that are present in the reference molecule. Species variants are polynucleotide sequences that vary from one species to another. The resulting polypeptides will generally have significant amino acid identity relative to each other. A polymorphic variant is a variation in the polynucleotide sequence of a particular gene between individuals of a given species. Polymorphic variants also may encompass “single nucleotide polymorphisms” (SNPs) in which the polynucleotide sequence varies by one nucleotide base. The presence of SNPs may be indicative of, for example, a certain population, a disease state, or a propensity for a disease state.

[0184] A “variant” of a particular polypeptide sequence is defined as a polypeptide sequence having at least 40% sequence identity to the particular polypeptide sequence over a certain length of one of the polypeptide sequences using blastp with the “BLAST 2 Sequences” tool Version 2.0.9 (May 7, 1999) set at default parameters. Such a pair of polypeptides may show, for example, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% or greater sequence identity over a certain defined length of one of the polypeptides.

THE INVENTION

[0185] The invention is based on the discovery of new human receptors and membrane-associated proteins (REMAP), the polynucleotides encoding REMAP, and the use of these compositions for the diagnosis, treatment, or prevention of cardiovascular, neurological, gastrointestinal, lipid metabolism, cell proliferative, autoimmune/inflammatory, metabolic, developmental, and endocrine disorders.

[0186] Table 1 summarizes the nomenclature for the full length polynucleotide and polypeptide sequences of the invention. Each polynucleotide and its corresponding polypeptide are correlated to a single Incyte project identification number (Incyte Project ID). Each polypeptide sequence is denoted by both a polypeptide sequence identification number (Polypeptide SEQ ID NO:) and an Incyte polypeptide sequence number (Incyte Polypeptide ID) as shown. Each polynucleotide sequence is denoted by both a polynucleotide sequence identification number (Polynucleotide SEQ ID NO:) and an Incyte polynucleotide consensus sequence number (Incyte Polynucleotide ID) as shown.

[0187] Table 2 shows sequences with homology to the polypeptides of the invention as identified by BLAST analysis against the GenBank protein (genpept) database. Columns 1 and 2 show the polypeptide sequence identification number (Polypeptide SEQ ID NO:) and the corresponding Incyte polypeptide sequence number (Incyte Polypeptide ID) for polypeptides of the invention. Column 3 shows the GenBank identification number (GenBank ID NO:) of the nearest GenBank homolog. Column 4 shows the probability scores for the matches between each polypeptide and its homolog(s). Column 5 shows the annotation of the GenBank homolog(s) along with relevant citations where applicable, all of which are expressly incorporated by reference herein.

[0188] Table 3 shows various structural features of the polypeptides of the invention. Columns 1 and 2 show the polypeptide sequence identification number (SEQ ID NO:) and the corresponding Incyte polypeptide sequence number (Incyte Polypeptide ID) for each polypeptide of the invention. Column 3 shows the number of amino acid residues in each polypeptide. Column 4 shows potential phosphorylation sites, and column 5 shows potential glycosylation sites, as determined by the MOTIFS program of the GCG sequence analysis software package (Genetics Computer Group, Madison Wis.). Column 6 shows amino acid residues comprising signature sequences, domains, and motifs. Column 7 shows analytical methods for protein structure/function analysis and in some cases, searchable databases to which the analytical methods were applied.

[0189] Together, Tables 2 and 3 summarize the properties of polypeptides of the invention, and these properties establish that the claimed polypeptides are transmembrane proteins. For example, SEQ ID NO:21 is 52% identical, from residue G14 to residue E585, to the rat, C2 domain-containing, transmembrane protein, GLUT4 (GenBank ID g4193489), as determined by the Basic Local Alignment Search Tool (BLAST). (See Table 2.) The BLAST probability score is 6.8e-192, which indicates the probability of obtaining the observed polypeptide sequence alignment by chance. SEQ ID NO:21 also contains C2 domains as determined by searching for statistically significant matches in the hidden Markov model (HMM)-based PFAM database of conserved protein family domains. (See Table 3.) Data from B:OMPS and PROFILESCAN analyses provide further corroborative evidence that SEQ ID NO:21 is a C2 domain-containing transmembrane protein.

[0190] In an alternative example, SEQ ID NO:27 is 97% identical, from residue M1 to residue K115, to human vesicle associated membrane protein-1B (GenBank ID g3372648) as determined by the Basic Local Alignment Search Tool (BLAST). (See Table 2.) The BLAST probability score is 4.2e-55, which indicates the probability of obtaining the observed polypeptide sequence alignment by chance. SEQ ID NO:27 also contains a synaptobrevin domain as determined by searching for statistically significant matches in the hidden Markov model (M)-based PFAM database of conserved protein family domains. (See Table 3.) Data from BUMPS, MOTIFS, and PROFILESCAN analyses provide further corroborative evidence that SEQ ID NO:27 is a synaptobrevin (note that “synaptobrevin” is another name for the vesicle-associated membrane protein (VAMP) family of membrane trafficking proteins).

[0191] In an alternative example, SEQ ID NO:30 is 99% identical from residue M323 to residue Y848 (62% identical over the full length of SEQ ID NO:30) to human delayed-rectifier potassium channel alpha subunit (GenBank ED g2815901) as determined by the Basic Local Alignment Search Tool (BLAST). (See Table 2.) The BLAST probability score is 9.1e-284, which indicates the probability of obtaining the observed polypeptide sequence alignment by chance. SEQ ID NO:30 also contains a potassium channel tetramerization domain as determined by searching for statistically significant matches in the hidden Markov model (HMM)-based PFAM database of conserved protein family domains. (See Table 3.) Data from BUMPS and MOTIFS analyses provide further corroborative evidence that SEQ ID NO30 is a potassium channel protein.

[0192] In an alternative example, SEQ ID NO:37 is 32% identical from residue G477 to residue L683, and 32% identical from residue K41 to residue L216, to human HERC2 (GenBank ID g4079809) as determined by the Basic Local Alignment Search Tool (BLAST). (See Table 2.) The BLAST probability score is 3.3e-25, which indicates the probability of obtaining the observed polypeptide sequence alignment by chance. SEQ ID NO:37 also contains a membrane occupation and recognition nexus repeat as determined by searching for statistically significant matches in the hidden Markov model (HMM)-based PFAM database of conserved protein family domains. (See Table 3.) Data from BLIMPS, MOTIFS, and PROFILESCAN analyses provide further corroborative evidence that SEQ ID NO:37 is a GTP dissociation factor.

[0193] The algorithms and parameters for the analysis of SEQ ID NO:1-20, SEQ ID NO:22-26, SEQ ID NO:28-29, SEQ ID NO:31-36, and SEQ ID NO:38-43 were analyzed and annotated in a similar manner and are described in Table 7.

[0194] As shown in Table 4, the full length polynucleotide sequences of the present invention were assembled using cDNA sequences or coding (exon) sequences derived from genomic DNA, or any combination of these two types of sequences. Column 1 lists the polynucleotide sequence identification number (Polynucleotide SEQ ID NO:), the corresponding Incyte polynucleotide consensus sequence number (Incyte ID) for each polynucleotide of the invention, and the length of each polynucleotide sequence in basepairs. Column 2 shows the nucleotide start (5′) and stop (3′) positions of the cDNA and/or genomic sequences used to assemble the full length polynucleotide sequences of the invention, and of fragments of the polynucleotide sequences which are useful, for example, in hybridization or amplification technologies that identify SEQ ID NO:44-86 or that distinguish between SEQ ID NO:44-86 and related polynucleotide sequences.

[0195] The polynucleotide fragments described in Column 2 of Table 4 may refer specifically, for example, to bicyte cDNAs derived from tissue-specific cDNA libraries or from pooled cDNA libraries. Alternatively, the polynucleotide fragments described in column 2 may refer to GenBank cDNAs or ESTs which contributed to the assembly of the full length polynucleotide sequences. In addition, the polynucleotide fragments described in column 2 may identify sequences derived from the ENSEMBL (The Sanger Centre, Cambridge, UK) database (i.e., those sequences including the designation “ENST”). Alternatively, the polynucleotide fragments described in column 2 may be derived from the NCBI RefSeq Nucleotide Sequence Records Database (i.e., those sequences including the designation “NM” or “NT”) or the NCBI RefSeq Protein Sequence Records (i.e., those sequences including the designation “NP”). Alternatively, the polynucleotide fragments described in column 2 may refer to assemblages of both cDNA and Genscan-predicted exons brought together by an “exon stitching” algorithm. For example, a polynucleotide sequence identified as FL_XXXXXX_N_(1—)N_(2—)YYYYY_N_(3—)N₄ represents a “stitched” sequence in which XXXXXX is the identification number of the cluster of sequences to which the algorithm was applied, and YYYYY is the number of the prediction generated by the algorithm, and N_(1,2,3 . . .) , if present, represent specific exons that may have been manually edited during analysis (See Example V). Alternatively, the polynucleotide fragments in column 2 may refer to assemblages of exons brought together by an “exon-stretching” algorithm. For example, a polynucleotide sequence identified as FLXXXXXX_gAAAAA_gBBBBB_(—)1_N is a “stretched” sequence, with XXXXXX being the Incyte project identification number, gAAAAA being the GenBank identification number of the human genomic sequence to which the “exon-stretching” algorithm was applied, gBBBBB being the GenBank identification number or NCBI RefSeq identification number of the nearest GenBank protein homolog, and N referring to specific exons (See Example V). In instances where a RefSeq sequence was used as a protein homolog for the “exon-stretching” algorithm, a RefSeq identifier (denoted by “NM,” “NP,” or “NT”) may be used in place of the GenBank identifier (i.e., gBBBBB).

[0196] Alternatively, a prefix identifies component sequences that were hand-edited, predicted from genomic DNA sequences, or derived from a combination of sequence analysis methods. The following Table lists examples of component sequence prefixes and corresponding sequence analysis methods associated with the prefixes (see Example IV and Example V). Prefix Type of analysis and/or examples of programs GNN, Exon prediction from genomic sequences using, for example, GFG, GENSCAN (Stanford University, CA, USA) or FGENES ENST (Computer Genomics Group, The Sanger Centre, Cambridge, UK) GBI Hand-edited analysis of genomic sequences. FL Stitched or stretched genomic sequences (see Example V). INCY Full length transcript and exon prediction from mapping of EST sequences to the genome. Genomic location and EST composition data are combined to predict the exons and resulting transcript.

[0197] In some cases, Incyte cDNA coverage redundant with the sequence coverage shown in Table 4 was obtained to confirm the final consensus polynucleotide sequence, but the relevant Incyte cDNA identification numbers are not shown.

[0198] Table 5 shows the representative cDNA libraries for those full length polynucleotide sequences which were assembled using Incyte cDNA sequences. The representative cDNA library is the Incyte cDNA library which is most frequently represented by the Incyte cDNA sequences which were used to assemble and confirm the above polynucleotide sequences. The tissues and vectors which were used to construct the cDNA libraries shown in Table 5 are described in Table 6.

[0199] The invention also encompasses REMAP variants. A preferred REMAP variant is one which has at least about 80%, or alternatively at least about 90%, or even at least about 95% amino acid sequence identity to the REMAP amino acid sequence, and which contains at least one functional or structural characteristic of REMAP.

[0200] The invention also encompasses polynucleotides which encode REMAP. In a particular embodiment, the invention encompasses a polynucleotide sequence comprising a sequence selected from the group consisting of SEQ ID NO:44-86, which encodes REMAP. The polynucleotide sequences of SEQ ID NO:44-86, as presented in the Sequence Listing, embrace the equivalent RNA sequences, wherein occurrences of the nitrogenous base thymine are replaced with uracil, and the sugar backbone is composed of ribose instead of deoxyribose.

[0201] The invention also encompasses a variant of a polynucleotide sequence encoding REMAP. In particular, such a variant polynucleotide sequence will have at least about 70%, or alternatively at least about 85%, or even at least about 95% polynucleotide sequence identity to the polynucleotide sequence encoding REMAP. A particular aspect of the invention encompasses a variant of a polynucleotide sequence comprising a sequence selected from the group consisting of SEQ ID NO:44-86 which has at least about 70%, or alternatively at least about 85%, or even at least about 95% polynucleotide sequence identity to a nucleic acid sequence selected from the group consisting of SEQ ID NO:44-86. Any one of the polynucleotide variants described above can encode an amino acid sequence which contains at least one functional or structural characteristic of REMAP.

[0202] In addition, or in the alternative, a polynucleotide variant of the invention is a splice variant of a polynucleotide sequence encoding REMAP. A splice variant may have portions which have significant sequence identity to the polynucleotide sequence encoding REMAP, but will generally have a greater or lesser number of polynucleotides due to additions or deletions of blocks of sequence arising from alternate splicing of exons during mRNA processing. A splice variant may have less than about 70%, or alternatively less than about 60%, or alternatively less than about 50% polynucleotide sequence identity to the polynucleotide sequence encoding REMAP over its entire length; however, portions of the splice variant will have at least about 70%, or alternatively at least about 85%, or alternatively at least about 95%, or alternatively 100% polynucleotide sequence identity to portions of the polynucleotide sequence encoding REMAP. For example, a polynucleotide comprising a sequence of SEQ ID NO:85 is a splice variant of a polynucleotide comprising a sequence of SEQ ID NO:84. In an alternative example, a polynucleotide comprising a sequence of SEQ ID NO:86 is a splice variant of a polynucleotide comprising a sequence of SEQ ID NO:71. Any one of the splice variants described above can encode an amino acid sequence which contains at least one functional or structural characteristic of REMAP.

[0203] It will be appreciated by those skilled in the art that as a result of the degeneracy of the genetic code, a multitude of polynucleotide sequences encoding REMAP, some bearing minimal similarity to the polynucleotide sequences of any known and naturally occurring gene, may be produced. Thus, the invention contemplates each and every possible variation of polynucleotide sequence that could be made by selecting combinations based on possible codon choices. These combinations are made in accordance with the standard triplet genetic code as applied to the polynucleotide sequence of naturally occurring REMAP, and all such variations are to be considered as being specifically disclosed.

[0204] Although nucleotide sequences which encode REMAP and its variants are generally capable of hybridizing to the nucleotide sequence of the naturally occurring REMAP under appropriately selected conditions of stringency, it may be advantageous to produce nucleotide sequences encoding REMAP or its derivatives possessing a substantially different codon usage, e.g., inclusion of non-naturally occurring codons. Codons may be selected to increase the rate at which expression of the peptide occurs in a particular prokaryotic or eukaryotic host in accordance with the frequency with which particular codons are utilized by the host. Other reasons for substantially altering the nucleotide sequence encoding REMAP and its derivatives without altering the encoded amino acid sequences include the production of RNA transcripts having more desirable properties, such as a greater half-life, than transcripts produced from the naturally occurring sequence.

[0205] The invention also encompasses production of DNA sequences which encode REMAP and REMAP derivatives, or fragments thereof, entirely by synthetic chemistry. After production, the synthetic sequence may be inserted into any of the many available expression vectors and cell systems using reagents well known in the art. Moreover, synthetic chemistry may be used to introduce mutations into a sequence encoding REMAP or any fragment thereof.

[0206] Also encompassed by the invention are polynucleotide sequences that are capable of hybridizing to the claimed polynucleotide sequences, and, in particular, to those shown in SEQ ID NO:44-86 and fragments thereof under various conditions of stringency. (See, e.g., Wahl, G. M. and S. L. Berger (1987) Methods Enzymol. 152:399407; Kimmel, A. R. (1987) Methods Enzymol. 152:507-511.) Hybridization conditions, including annealing and wash conditions, are described in “Definitions.”

[0207] Methods for DNA sequencing are well known in the art and may be used to practice any of the embodiments of the invention. The methods may employ such enzymes as the Klenow fragment of DNA polymerase I, SEQUENASE (US Biochemical, Cleveland Ohio), Taq polymerase (Applied Biosystems), thermostable T7 polymerase (Amersham Pharmacia Biotech, Piscataway N.J.), or combinations of polymerase and proofreading exonucleases such as those found in the ELONGASE amplification system (i.e. Technologies, Gaithersburg Md.). Preferably, sequence preparation is automated with machines such as the MICROLAB 2200 liquid transfer system (Hamilton, Reno Nev.), PTC200 thermal cycler (MJ Research, Watertown Mass.) and ABI CATALYST 800 thermal cycler (Applied Biosystems). Sequencing is then carried out using either the ABI 373 or 377 DNA sequencing system (Applied Biosystems), the MEGABACE 1000 DNA sequencing system (Molecular Dynamics, Sunnyvale Calif.), or other systems known in the art. The resulting sequences are analyzed using a variety of algorithms which are well known in the art (See, e.g., Ausubel, F. M. (1997) Short Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., unit 7.7; Meyers, R. A. (1995) Molecular Biology and Biotechnology, Wiley VCH, New York N.Y., pp.856-853.)

[0208] The nucleic acid sequences encoding REMAP maybe extended utilizing a partial nucleotide sequence and employing various PCR-based methods known in the art to detect upstream sequences, such as promoters and regulatory elements. For example, one method which maybe employed, restriction-site PCR, uses universal and nested primers to amplify unknown sequence from genomic DNA within a cloning vector. (See, e.g., Sarkar, G. (1993) PCR Methods Applic. 2:318-322.) Another method, inverse PCR, uses primers that extend in divergent directions to amplify unknown sequence from a circularized template. The template is derived from restriction fragments comprising a known genomic locus and surrounding sequences. (See, e.g., Triglia, T. et al. (1988) Nucleic Acids Res. 16:8186.) A third method, capture PCR, involves PCR amplification of DNA fragments adjacent to known sequences inhuman and yeast artificial chromosome DNA. (See, e.g., Lagerstrom, M. et al. (1991) PCR Methods Applic. 1:111-119.) In this method, multiple restriction enzyme digestions and ligations maybe used to insert an engineered double-stranded sequence into a region of unknown sequence before performing PCR. Other methods which may be used to retrieve unknown sequences are known in the art. (See, e.g., Parker, J. D. et al. (1991) Nucleic Acids Res. 19:3055-3060). Additionally, one may use PCR, nested primers, and PROMOTERFINDER libraries (Clontech, Palo Alto Calif.) to walk genomic DNA. This procedure avoids the need to screen libraries and is useful in finding intron/exon junctions. For all PCR-based methods, primers may be designed using commercially available software, such as OLIGO 4.06 primer analysis software (National Biosciences, Plymouth Minn.) or another appropriate program, to be about 22 to 30 nucleotides in length, to have a GC content of about 50% or more, and to anneal to the template at temperatures of about 68° C. to 72° C.

[0209] When screening for full length cDNAs, it is preferable to use libraries that have been size-selected to include larger cDNAs. In addition, random-primed libraries, which often include sequences containing the 5′regions of genes, are preferable for situations in which an oligo d(T) library does not yield a full-length cDNA. Genomic libraries may be useful for extension of sequence into 5′non-transcribed regulatory regions.

[0210] Capillary electrophoresis systems which are commercially available may be used to analyze the size or confirm the nucleotide sequence of sequencing or PCR products. In particular, capillary sequencing may employ flowable polymers for electrophoretic separation, four different nucleotide-specific, laser-stimulated fluorescent dyes, and a charge coupled device camera for detection of the emitted wavelengths. Output/light intensity may be converted to electrical signal using appropriate software (e.g., GENOTYPER and SEQUENCE NAVIGATOR, Applied Biosystems), and the entire process from loading of samples to computer analysis and electronic data display may be computer controlled. Capillary electrophoresis is especially preferable for sequencing small DNA fragments which may be present in limited amounts in a particular sample.

[0211] In another embodiment of the invention, polynucleotide sequences or fragments thereof which encode REMAP may be cloned in recombinant DNA molecules that direct expression of REMAP, or fragments or functional equivalents thereof, in appropriate host cells. Due to the inherent degeneracy of the genetic code, other DNA sequences which encode substantially the same or a functionally equivalent amino acid sequence maybe produced and used to express REMAP.

[0212] The nucleotide sequences of the present invention can be engineered using methods generally known in the art in order to alter REMAP-encoding sequences for a variety of purposes including, but not limited to, modification of the cloning, processing, and/or expression of the gene product DNA shuffling by random fragmentation and PCR reassembly of gene fragments and synthetic oligonucleotides may be used to engineer the nucleotide sequences. For example, oligonucleotide-mediated site-directed mutagenesis may be used to introduce mutations that create new restriction sites, alter glycosylation patterns, change codon preference, produce splice variants, and so forth.

[0213] The nucleotides of the present invention may be subjected to DNA shuffling techniques such as MOLECULARBREEDING (Maxygen Inc., Santa Clara Calif.; described in U.S. Pat. No. 5,837,458; Chang, C.-C. et al. (1999) Nat. Biotechnol. 17:793-797; Christians, F. C. et al. (1999) Nat. Biotechnol. 17:259-264; and Crameri, A. et al. (1996) Nat. Biotechnol. 14:315-319) to alter or improve the biological properties of REMAP, such as its biological or enzymatic activity or its ability to bind to other molecules or compounds. DNA shuffling is a process by which a library of gene variants is produced using PCR-mediated recombination of gene fragments. The library is then subjected to selection or screening procedures that identify those gene variants with the desired properties. These preferred variants may then be pooled and further subjected to recursive rounds of DNA shuffling and selection/screening. Thus, genetic diversity is created through “artificial” breeding and rapid molecular evolution. For example, fragments of a single gene containing random point mutations may be recombined, screened, and then reshuffled until the desired properties are optimized. Alternatively, fragments of a given gene may be recombined with fragments of homologous genes in the same gene family, either from the same or different species, thereby maximizing the genetic diversity of multiple naturally occurring genes in a directed and controllable manner.

[0214] In another embodiment, sequences encoding REMAP may be synthesized, in whole or in part, using chemical methods well known in the art. (See, e.g., Caruthers, M. H. et al. (1980) Nucleic Acids Symp. Ser. 7:215-223; and Horn, T. et al. (1980) Nucleic Acids Symp. Ser. 7:225-232.) Alternatively, REMAP itself or a fragment thereof may be synthesized using chemical methods. For example, peptide synthesis can be performed using various solution-phase or solid-phase techniques. (See, e.g., Creighton, T. (1984) Proteins Structures and Molecular Properties, WH Freeman, New York N.Y., pp. 55-60; and Roberge, J. Y. et al. (1995) Science 269:202-204.) Automated synthesis maybe achieved using the ABI 43 1A peptide synthesizer (Applied Biosystems). Additionally, the amino acid sequence of REMAP, or any part thereof, may be altered during direct synthesis and/or combined with sequences from other proteins, or any part thereof, to produce a variant polypeptide or a polypeptide having a sequence of a naturally occurring polypeptide.

[0215] The peptide may be substantially purified by preparative high performance liquid chromatography. (See, e.g., Chiez, R. M. and F. Z. Regnier (1990) Methods Enzymol. 182:392-421.) The composition of the synthetic peptides may be confirmed by amino acid analysis or by sequencing. (See, e.g., Creighton, supra, pp. 28-53.)

[0216] In order to express a biologically active REMAP, the nucleotide sequences encoding REMAP or derivatives thereof may be inserted into an appropriate expression vector, i.e., a vector which contains the necessary elements for transcriptional and translational control of the inserted coding sequence in a suitable host. These elements include regulatory sequences, such as enhancers, constitutive and inducible promoters, and 5′ and 3′ untranslated regions in the vector and in polynucleotide sequences encoding REMAP. Such elements may vary in their strength and specificity. Specific initiation signals may also be used to achieve more efficient translation of sequences encoding REMAP. Such signals include the ATG initiation codon and adjacent sequences, e.g. the Kozak sequence. In cases where sequences encoding REMAP and its initiation codon and upstream regulatory sequences are inserted into the appropriate expression vector, no additional transcriptional or translational control signals may be needed. However, in cases where only coding sequence, or a fragment thereof, is inserted, exogenous translational control signals including an in-frame ATG initiation codon should be provided by the vector. Exogenous translational elements and initiation codons may be of various origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of enhancers appropriate for the particular host cell system used. (See, e.g., Scharf, D. et al. (1994) Results Probl. Cell Differ. 20:125-162.)

[0217] Methods which are well known to those skilled in the art may be used to construct expression vectors containing sequences encoding REMAP and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. (See, e.g., Sambrook, J. et al. (1989) Molecular Cloning. A Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y., ch. 4, 8, and 16-17; Ausubel, F. M. et al. (1995) Current Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., ch. 9, 13, and 16.)

[0218] A variety of expression vector/host systems may be utilized to contain and express sequences encoding REMAP. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with viral expression vectors (e.g., baculovirus); plant cell systems transformed with viral expression vectors (e.g., cauliflower mosaic virus, CaMV, or tobacco mosaic virus, TMV) or with bacterial expression vectors (e.g., Ti or pBR322 plasmids); or animal cell systems. (See, e.g., Sambrook, supra; Ausubel, supra; Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509; Engelhard, E. K. et al. (1994) Proc. Natl. Acad. Sci. USA 91:3224-3227; Sandig, V. et al. (1996) Hum. Gene Ther. 7:1937-1945; Takamatsu, N. (1987) EMBO J. 6:307-311; The McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York N.Y., pp. 191-196; Logan, J. and T. Shenk (1984) Proc. Natl. Acad. Sci. USA 81:3655-3659; and Harrington, J. J. et al. (1997) Nat. Genet. 15:345-355.) Expression vectors derived from retroviruses, adenoviruses, or herpes or vaccinia viruses, or from various bacterial plasmids, may be used for delivery of nucleotide sequences to the targeted organ, tissue, or cell population. (See, e.g., Di Nicola, M. et al. (1998) Cancer Gen. Ther. 5(6):350-356; Yu, M. et al. (1993) Proc. Natl. Acad. Sci. USA 90(13):6340-6344; Buller, R. M. et al (1985) Nature 317(6040):813-815; McGregor, D. P. et al. (1994) Mol. Immunol. 31(3):219-226; and Verma, I. M. and N. Somia (1997) Nature 389:239-242.) The invention is not limited by the host cell employed.

[0219] In bacterial systems, a number of cloning and expression vectors may be selected depending upon the use intended for polynucleotide sequences encoding REMAP. For example, routine cloning, subcloning, and propagation of polynucleotide sequences encoding REMAP can be achieved using a multifunctional E. coli vector such as PBLUESCRIPT (Stratagene, La Jolla Calif.) or PSPORT1 plasmid (Life Technologies). Ligation of sequences encoding REMAP into the vector's multiple cloning site disrupts the lacZ gene, allowing a colorimetric screening procedure for identification of transformed bacteria containing recombinant molecules. In addition, these vectors may be useful for in vitro transcription, dideoxy sequencing, single strand rescue with helper phage, and creation of nested deletions in the cloned sequence. (See, e.g., Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509.) When large quantities of REMAP are needed, e.g. for the production of antibodies, vectors which direct high level expression of REMAP may be used. For example, vectors containing the strong, inducible SP6 or 17 bacteriophage promoter may be used.

[0220] Yeast expression systems may be used for production of REMAP. A number of vectors containing constitutive or inducible promoters, such as alpha factor, alcohol oxidase, and PGH promoters, may be used in the yeast Saccharomyces cerevisiae or Pichia pastoris. In addition, such vectors direct either the secretion or intracellular retention of expressed proteins and enable integration of foreign sequences into the host genome for stable propagation. (See, e.g., Ausubel, 1995, supra; Bitter, G. A. et al. (1987) Methods Enzymol. 153:516-544; and Scorer, C. A. et al. (1994) Bio/Technology 12:181-184.)

[0221] Plant systems may also be used for expression of REMAP. Transcription of sequences encoding REMAP may be driven by viral promoters, e.g., the 35S and 19S promoters of CaMV used alone or in combination with the omega leader sequence from TMV (Takamatsu, N. (1987) EMBO J. 6:307-311). Alternatively, plant promoters such as the small subunit of RUBISCO or heat shock promoters may be used. (See, e.g., Coruzzi, G. et al. (1984) EMBO J. 3:1671-1680; Broglie, R. et al. (1984) Science 224:838-843; and Winter, J. et al. (1991) Results Probl. Cell Differ. 17:85-105.) These constructs can be introduced into plant cells by direct DNA transformation or pathogen-mediated transfection. (See, e.g., The McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York N.Y., pp. 191-196.)

[0222] In mammalian cells, a number of viral-based expression systems may be utilized. In cases where an adenovirus is used as an expression vector, sequences encoding REMAP may be ligated into an adenovirus transcription/translation complex consisting of the late promoter and tripartite leader sequence. Insertion in a non-essential E1 or E3 region of the viral genome may be used to obtain infective virus which expresses REMAP inhost cells. (See, e.g., Logan, J. and T. Shenk (1984) Proc. Natl. Acad. Sci. USA 81:3655-3659.) In addition, transcription enhancers, such as the Rous sarcoma virus (RSV) enhancer, may be used to increase expression in mammalian host cells. SV40 or EBV-based vectors may also be used for high-level protein expression.

[0223] Human artificial chromosomes (HACs) may also be employed to deliver larger fragments of DNA than can be contained in and expressed from a plasmid. HACs of about 6 kb to 10 Mb are constructed and delivered via conventional delivery methods (liposomes, polycationic amino polymers, or vesicles) for therapeutic purposes. (See, e.g., Harrington, J. J. et al. (1997) Nat. Genet 15:345-355.)

[0224] For long term production of recombinant proteins in mammalian systems, stable expression of REMAP in cell lines is preferred. For example, sequences encoding REMAP can be transformed into cell lines using expression vectors which may contain viral origins of replication and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. Following the introduction of the vector, cells may be allowed to grow for about 1 to 2 days in enriched media before being switched to selective media. The purpose of the selectable marker is to confer resistance to a selective agent, and its presence allows growth and recovery of cells which successfully express the introduced sequences. Resistant clones of stably transformed cells may be propagated using tissue culture techniques appropriate to the cell type.

[0225] Any number of selection systems may be used to recover transformed cell lines. These include, but are not limited to, the herpes simplex virus thymidine kinase and adenine phosphoribosyltransferase genes, for use in tk and apr cells, respectively. (See, e.g., Wigler, M. et al. (1977) Cell 11:223-232; Lowy, I. et al. (1980) Cell 22:817-823.) Also, antiretabolite, antibiotic, or herbicide resistance can be used as the basis for selection. For example, dhfr confers resistance to methotrexate; neo confers resistance to the aminoglycosides neomycin and G-418; and als and pat confer resistance to chlorsulfuron and phosphinotricin acetyltransferase, respectively. (See, e.g., Wigler, M. et al. (1980) Proc. Natl. Acad. Sci. USA 77:3567-3570; Colbere-Garapin, F. et al. (1981) J. Mol. Biot 150:1-14.) Additional selectable genes have been described, e.g., trpB and hisD, which alter cellular requirements for metabolites. (See, e.g., Hartman, S. C. and R. C. Mulligan (1988) Proc. Natl. Acad. Sci. USA 85:8047-8051.) Visible markers, e.g., anthocyanins, green fluorescent proteins (GFP; Clontech), β glucuronidase and its substrate β-glucuronide, or luciferase and its substrate luciferin may be used. These markers can be used not only to identify transformants, but also to quantify the amount of transient or stable protein expression attributable to a specific vector system. (See, e.g., Rhodes, C. A. (1995) Methods Mol. Biol. 55:121-131.)

[0226] Although the presence/absence of marker gene expression suggests that the gene of interest is also present, the presence and expression of the gene may need to be confirmed. For example, if the sequence encoding REMAP is inserted within a marker gene sequence, transformed cells containing sequences encoding REMAP can be identified by the absence of marker gene function. Alternatively, a marker gene can be placed in tandem with a sequence encoding REMAP under the control of a single promoter. Expression of the marker gene in response to induction or selection usually indicates expression of the tandem gene as well.

[0227] In general, host cells that contain the nucleic acid sequence encoding REMAP and that express REMAP may be identified by a variety of procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations, PCR amplification, and protein bioassay or immunoassay techniques which include membrane, solution, or chip based technologies for the detection and/or quantification of nucleic acid or protein sequences.

[0228] Immunological methods for detecting and measuring the expression of REMAP using either specific polyclonal or monoclonal antibodies are known in the art. Examples of such techniques include enzyme-linked immunosorbent assays (ELISAs), radioimmunoassays (RIAs), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes on REMAP is preferred, but a competitive binding assay may be employed. These and other assays are well known in the art. (See, e.g., Hampton, R. et al. (1990) Serologcal Methods, a Laboratory Manual, APS Press, St. Paul Minn., Sect. IV; Coligan, J. E. et al. (1997) Current Protocols in Immunology, Greene Pub. Associates and Wiley-Interscience, New York N.Y.; and Pound, J. D. (1998) Immunochemical Protocols, Humana Press, Totowa N.J.)

[0229] A wide variety of labels and conjugation techniques are known by those skilled in the art and may be used in various nucleic acid and amino acid assays. Means for producing labeled hybridization or PCR probes for detecting sequences related to polynucleotides encoding REMAP include oligolabeling, nick translation, end-labeling, or PCR amplification using a labeled nucleotide. Alternatively, the sequences encoding REMAP, or any fragments thereof, may be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase such as T7, T3, or SP6 and labeled nucleotides. These procedures may be conducted using a variety of commercially available kits, such as those provided by Amersham Pharmacia Biotech, Promega (Madison Wis.), and US Biochemical. Suitable reporter molecules or labels which may be used for ease of detection include radionuclides, enzymes, fluorescent, chemiluminescent, or chromogenic agents, as well as substrates, cofactors, inhibitors, magnetic particles, and the like.

[0230] Host cells transformed with nucleotide sequences encoding REMAP may be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The protein produced by a transformed cell may be secreted or retained intracellularly depending on the sequence and/or the vector used. As will be understood by those of skill in the art, expression vectors containing polynucleotides which encode REMAP maybe designed to contain signal sequences which direct secretion of REMAP through a prokaryotic or eukaryotic cell membrane.

[0231] In addition, a host cell strain may be chosen for its ability to modulate expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” or “pro” form of the protein may also be used to specify protein targeting, folding, and/or activity. Different host cells which have specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO, HeLa, MDCK, HEK293, and W138) are available from the American Type Culture Collection (ATCC, Manassas Va.) and may be chosen to ensure the correct modification and processing of the foreign protein.

[0232] In another embodiment of the invention, natural, modified, or recombinant nucleic acid sequences encoding REMAP may be ligated to a heterologous sequence resulting in translation of a fusion protein in any of the aforementioned host systems. For example, a chimeric REMAP protein containing a heterologous moiety that can be recognized by a commercially available antibody may facilitate the screening of peptide libraries for inhibitors of REMAP activity. Heterologous protein and peptide moieties may also facilitate purification of fusion proteins using commercially available affinity matrices. Such moieties include, but are not limited to, glutathione S-transferase (GST), maltose binding protein (MBP), thioredoxin (Trx), calmodulin binding peptide (CBP), 6-His, FLAG, c-myc, and hemagglutinin (HA). GST, MBP, Trx, CBP, and 6-His enable purification of their cognate fusion proteins on immobilized glutathione, maltose, phenylarsine oxide, calmodulin, and metal-chelate resins, respectively. FLAG, c-myc, and hemagglutinin (HA) enable immunoaffinity purification of fusion proteins using commercially available monoclonal and polyclonal antibodies that specifically recognize these epitope tags. A fusion protein may also be engineered to contain a proteolytic cleavage site located between the REMAP encoding sequence and the heterologous protein sequence, so that REMAP may be cleaved away from the heterologous moiety following purification. Methods for fusion protein expression and purification are discussed in Ausubel (1995, supra, ch. 10). A variety of commercially available kits may also be used to facilitate expression and purification of fusion proteins.

[0233] In a further embodiment of the invention, synthesis of radiolabeled REMAP maybe achieved in vitro using the TNT rabbit reticulocyte lysate or wheat germ extract system (Promega). These systems couple transcription and translation of protein-coding sequences operably associated with the T7, T3, or SP6 promoters. Translation takes place in the presence of a radiolabeled amino acid precursor, for example, ³⁵S-methionine.

[0234] REMAP of the present invention or fragments thereof may be used to screen for compounds that specifically bind to REMAP. At least one and up to a plurality of test compounds may be screened for specific binding to REMAP. Examples of test compounds include antibodies, oligonucleotides, proteins (e.g., receptors), or small molecules.

[0235] In one embodiment, the compound thus identified is closely related to the natural ligand of REMAP, e.g., a ligand or fragment thereof, a natural substrate, a structural or functional mimetic, or a natural binding partner. (See, e.g., Coligan, J. E. et al. (1991) Current Protocols in Immunology 1(2): Chapter 5.) Similarly, the compound can be closely related to the natural receptor to which REMAP binds, or to at least a fragment of the receptor, e.g., the ligand binding site. In either case, the compound can be rationally designed using known techniques. In one embodiment, screening for these compounds involves producing appropriate cells which express REMAP, either as a secreted protein or on the cell membrane. Preferred cells include cells from mammals, yeast, Drosophila, or E. coli. Cells expressing REMAP or cell membrane fractions which contain REMAP are then contacted with a test compound and binding, stimulation, or inhibition of activity of either REMAP or the compound is analyzed.

[0236] An assay may simply test binding of a test compound to the polypeptide, wherein binding is detected by a fluorophore, radioisotope, enzyme conjugate, or other detectable label. For example, the assay may comprise the steps of combining at least one test compound with REMAP, either in solution or affixed to a solid support, and detecting the binding of REMAP to the compound. Alternatively, the assay may detect or measure binding of a test compound in the presence of a. labeled competitor. Additionally, the assay may be carried out using cell-free preparations, chemical libraries, or natural product mixtures, and the test compound(s) may be free in solution or affixed to a solid support.

[0237] REMAP of the present invention or fragments thereof may be used to screen for compounds that modulate the activity of REMAP. Such compounds may include agonists, antagonists, or partial or inverse agonists. In one embodiment, an assay is performed under conditions permissive for REMAP activity, wherein REMAP is combined with at least one test compound, and the activity of REMAP in the presence of a test compound is compared with the activity of REMAP in the absence of the test compound. A change in the activity of REMAP in the presence of the test compound is indicative of a compound that modulates the activity of REMAP. Alternatively, a test compound is combined with an in vitro or cell-free system comprising REMAP under conditions suitable for REMAP activity, and the assay is performed. In either of these assays, a test compound which modulates the activity of REMAP may do so indirectly and need not come in direct contact with the test compound. At least one and up to a plurality of test compounds may be screened.

[0238] In another embodiment, polynucleotides encoding REMAP or their mammalian homologs may be “Knocked out” in an animal model system using homologous recombination in embryonic stem (ES) cells. Such techniques are well known in the art and are useful for the generation of animal models of human disease. (See, e.g., U.S. Pat. No. 5,175,383 and U.S. Pat. No. 5,767,337.) For example, mouse ES cells, such as the mouse 129/SvJ cell line, are derived from the early mouse embryo and grown in culture. The ES cells are transformed with a vector containing the gene of interest disrupted by a marker gene, e.g., the neomycin phosphotransferase gene (neo; Capecchi, M. R. (1989) Science 244:1288-1292). The vector integrates into the corresponding region of the host genome by homologous recombination. Alternatively, homologous recombination takes place using the Cre-loxP system to knockout a gene of interest in a tissue- or developmental stage-specific manner (Marth, J. D. (1996) Clin. Invest. 97:1999-2002; Wagner, K. U. et al. (1997) Nucleic Acids Res. 25:4323-4330). Transformed ES cells are identified and microinjected into mouse cell blastocysts such as those from the C57BL/6 mouse strain. The blastocysts are surgically transferred to pseudopregnant dams, and the resulting chimeric progeny are genotyped and bred to produce heterozygous or homozygous strains. Transgenic animals thus generated may be tested with potential therapeutic or toxic agents.

[0239] Polynucleotides encoding REMAP may also be manipulated in vitro in ES cells derived from human blastocysts. Human ES cells have the potential to differentiate into at least eight separate cell lineages including endoderm, mesoderm, and ectodermal cell types. These cell lineages differentiate into, for example, neural cells, hematopoietic lineages, and cardiomyocytes (Thomson, J. A. et al. (1998) Science 282:1145-1147).

[0240] Polynucleotides encoding REMAP can also be used to create “knockin” humanized animals (pigs) or transgenic animals (mice or rats) to model human disease. With knockin technology, a region of a polynucleotide encoding REMAP is injected into animal ES cells, and the injected sequence integrates into the animal cell genome. Transformed cells are injected into blastulae, and the blastulae are implanted as described above. Transgenic progeny or inbred lines are studied and treated with potential pharmaceutical agents to obtain information on treatment of a human disease. Alternatively, a mammal inbred to overexpress REMAP, e.g., by secreting REMAP in its milk, may also serve as a convenient source of that protein (Janne, J. et al. (1998) Biotechnol Annu. Rev. 4:55-74).

[0241] Therapeutics

[0242] Chemical and structural similarity, e.g., in the context of sequences and motifs, exists between regions of REMAP and receptors and membrane-associated proteins. In addition, examples of tissues expressing REMAP closely associated with a number of diseased tissues, including but not limited to those of the heart, lung, kidney, liver, brain, digestive, pituitary, and prostate tissues, increased transmembrane protein expression or activity, normal and cancerous breast and colon tissues, normal and obese adipocytes, Tangier disease-derived fibroblasts and normal fibroblasts, and can also be found in Table 6. Therefore, REMAP appears to play a role in cardiovascular, neurological, gastrointestinal, lipid metabolism, cell proliferative, autoimmune/inflammatory, metabolic, developmental, and endocrine disorders. In the treatment of disorders associated with increased REMAP expression or activity, it is desirable to decrease the expression or activity of REMAP. In the treatment of disorders associated with decreased REMAP expression or activity, it is desirable to increase the expression or activity of REMAP.

[0243] Therefore, in one embodiment, REMAP or a fragment or derivative thereof maybe administered to a subject to treat or prevent a disorder associated with decreased expression or activity of REMAP. Examples of such disorders include, but are not limited to, a cardiovascular disorder including blood vessel disorders such as arteriovenous fistula, atherosclerosis, hypertension, vasculitis, Raynaud's disease, aneurysms, arterial dissections, varicose veins, thrombophlebitis and pblebothrombosis, vascular tumors, and complications of thrombolysis, balloon angioplasty, vascular replacement, and coronary artery bypass graft surgery, heart disorders such as congestive heart failure, ischemic heart disease, angina pectoris, myocardial infarction, hypertensive heart disease, degenerative valvular heart disease, calcific aortic valve stenosis, congenitally bicuspid aortic valve, mitral annular calcification, mitral valve prolapse, rheumatic fever and rheumatic heart disease, infective endocarditis, nonbacterial thrombotic endocarditis, endocarditis of systemic lupus erythematosus, carcinoid heart disease, cardiomyopathy, myocarditis, pericarditis, neoplastic heart disease, congenital heart disease, and complications of cardiac transplantation, and lung disorders such as congenital lung anomalies, atelectasis, pulmonary congestion and edema, pulmonary embolism, pulmonary hemorrhage, pulmonary infarction, pulmonary hypertension, vascular sclerosis, obstructive pulmonary disease, restrictive pulmonary disease, chronic obstructive pulmonary disease, emphysema, chronic bronchitis, bronchial asthma, bronchiectasis, bacterial pneumonia, viral and mycoplasmal pneumonia, lung abscess, pulmonary tuberculosis, diffuse interstitial diseases, pneumoconioses, sarcoidosis, idiopathic pulmonary fibrosis, desquamative interstitial pneumonitis, hypersensitivity pneumonitis, pulmonary eosinophilia bronchiolitis obliterans-organizig pneumonia, diffuse pulmonary hemorrhage syndromes, Goodpasture's syndromes, idiopathic pulmonary hemosiderosis, pulmonary involvement in collagen-vascular disorders, pulmonary alveolar proteinosis, lung tumors, inflammatory and noninflammatory pleural effusions, pneumothorax, pleural tumors, drug-induced lung disease, radiation-induced lung disease, and complications of lung transplantation; a neurological disorder such as epilepsy, ischemic cerebrovascular disease, stroke, cerebral neoplasms, Alzheimer's disease, Pick's disease, Huntington's disease, dementia, Parkinson's disease and other extrapyramidal disorders, amyotrophic lateral sclerosis and other motor neuron disorders, progressive neural muscular atrophy, retinitis pigmentosa, hereditary ataxias, multiple sclerosis and other demyelinating diseases, bacterial and viral meningitis, brain abscess, subdural empyema, epidural abscess, suppurative intracranial thrombophlebitis, myelitis and radiculitis, viral central nervous system disease, prion diseases including kmru, Creutzfeldt-Jakob disease, and Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia, nutritional and metabolic diseases of the nervous system, neurofibromatosis, tuberous sclerosis, cerebelloretinal hemangioblastomatosis, encephalotrigeminal syndrome, mental retardation and other developmental disorders of the central nervous system, cerebral palsy, neuroskeletal disorders, autonomic nervous system disorders, cranial nerve disorders, spinal cord diseases, muscular dystrophy and other neuromuscular disorders, peripheral nervous system disorders, dermatomyositis and polymyositis, inherited, metabolic, endocrine, and toxic myopathies, myasthenia gravis, periodic paralysis, mental disorders including mood, anxiety, and schizophrenic disorders, seasonal affective disorder (SAD), akathesia, amnesia, catatonia, diabetic neuropathy, tardive dyskinesia, dystonias, paranoid psychoses, postherpetic neuralgia, Tourette's disorder, progressive supranuclear palsy, corticobasal degeneration, and familial frontotemporal dementia; a gastrointestinal disorder such as dysphagia, peptic esophagitis, esophageal spasm, esophageal stricture, esophageal carcinoma, dyspepsia, indigestion, gastritis, gastric carcinoma, anorexia, nausea, emesis, gastroparesis, antral or pyloric edema, abdominal angina, pyrosis, gastroenteritis, intestinal obstruction, infections of the intestinal tract, peptic ulcer, cholelithiasis, cholecystitis, cholestasis, pancreatitis, pancreatic carcinoma, biliary tract disease, hepatitis, hyperbilirubinemia, cirrhosis, passive congestion of the liver, hepatoma, infectious colitis, ulcerative colitis, ulcerative proctitis, Crohn's disease, Whipple's disease, Mallory-Weiss syndrome, colonic carcinoma, colonic obstruction, irritable bowel syndrome, short bowel syndrome, diarrhea, constipation, gastrointestinal hemorrhage, acquired immunodeficiency syndrome (AIDS) enteropathy, jaundice, hepatic encephalopathy, hepatorenal syndrome, hepatic steatosis, hemochromatosis, Wilson's disease, alpha₁-antitrypsin deficiency, Reye's syndrome, primary sclerosing cholangitis, liver infarction, portal vein obstruction and thrombosis, centrilobular necrosis, peliosis hepatis, hepatic vein thrombosis, veno-occlusive disease, preeclampsia, eclampsia, acute fatty liver of pregnancy, intrahepatic cholestasis of pregnancy, and hepatic tumors including nodular hyperplasias, adenomas, and carcinomas; a disorder of lipid metabolism such as fatty liver, cholestasis, primary biliary cirrhosis, carnitine deficiency, carnitine palmitoyltransferase deficiency, myoadenylate deaminase deficiency, hypertriglyceridemia, lipid storage disorders such Fabry's disease, Gaucher's disease, Niemann-Pick's disease, metachromatic leukodystrophy, adrenoleukodystrophy, GM₂ gangliosidosis, and ceroid lipofdscinosis, abetalipoproteinemia, Tangier disease, hyperlipoproteinemia, diabetes mellitus, lipodystrophy, lipomatoses, acute panniculitis, disseminated fat necrosis, adiposis dolorosa, lipoid adrenal hyperplasia, minimal change disease, lipomas, atherosclerosis, hypercholesterolemia, hypercholesterolemia with hypertriglyceridemia, primary hypoalphalipoproteinemia, hypothyroidism, renal disease, liver disease, lecithin:cholesterol acyltrafnserase deficiency, cerebrotendinous xanthomatosis, sitosterolemia, hypocholesterolemia, Tay-Sachs disease, Sandhoff's disease, hyperlipidemia, hyperlipemia, lipid myopathies, and obesity; a cell proliferative disorder such as actinic keratosis, arteriosclerosis, atherosclerosis, bursitis, cirrhosis, hepatitis, mixed connective tissue disease (MCTD), myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythermia vera, psoriasis, primary thrombocythemia, and cancers including adenocarcinoma, leukemia, lymphoma, melanoma, myeloma, sarcoma, teratocarcinoma, and, in particular, cancers of the adrenal gland, bladder, bone, bone marrow, brain, breast, cervix, gall bladder, ganglia, gastrointestinal tract, heart, kidney, liver, lung, muscle, ovary, pancreas, parathyroid, penis, prostate, salivary glands, skin, spleen, testis, thymus, thyroid, and uterus; an autoimmune/inflammatory disorder such as acquired immunodeficiency syndrome (AIDS), Addison's disease, adult respiratory distress syndrome, ankylosing spondylitis, amyloidosis, anemia, asthma, atherosclerosis, autoimmune hemolytic anemia, autoimmune thyroiditis, autoimmune polyenodocrinopathy-candidiasis-ectodermal dystrophy (APECED), bronchitis, cholecystitis, contact dermatitis, Crohn's disease, atopic dermatitis, dermatomyositis, diabetes mellitus, emphysema, episodic lymphopenia with lymphocytotoxins, erythroblastosis fetalis, erythema nodosum, atrophic gastritis, glomerulonephritis, Goodpasture's syndrome, gout, Graves' disease, Hashimoto's thyroiditis, hypereosinophilia, irritable bowel syndrome, multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, osteoarthritis, osteoporosis, pancreatitis, polymyositis, psoriasis, Reiter's syndrome, rheumatoid arthritis, scleroderma, Sjögren's syndrome, systemic anaphylaxis, systemic lupus erythematosus, systemic sclerosis, thrombocytopenic purpura, ulcerative colitis, uveitis, Werner syndrome, complications of cancer, hemodialysis, and extracorporeal circulation, viral, bacterial, fungal, parasitic, protozoal, and helminthic infections, and trauma; a metabolic disorder such as Addison's disease, cerebrotendinous xanthomatosis, congenital adrenal hyperplasia, coumnarin resistance, cystic fibrosis, fatty hepatocirrhosis, fructose-1,6-diphosphatase deficiency, galactosemia, goiter, glucagonoma, glycogen storage diseases, hereditary fructose intolerance, hyperadrenalism, hypoadrenalism, hyperparathyroidism, hypoparathyroidism, hypercholesterolemia, hyperthyroidism, hypoglycemia, hypothyroidism, hyperlipidenmia, hyperlipemita, lipid myopathies, lipodystrophies, lysosomal storage diseases, mannosidosis, neuraminidase deficiency, obesity, osteoporosis, phenylketonuria, pseudovitamin D-deficiency rickets, disorders of carbohydrate metabolism such as congenital type II dyserythropoietic anemia, diabetes, insulin-dependent diabetes melitus, non-insulin-dependent diabetes mellitus, galactose epimerase deficiency, glycogen storage diseases, lysosomal storage diseases, fructosuria, pentosuria, and inherited abnormalities of pyruvate metabolism, disorders of lipid metabolism such as fatty liver, cholestasis, primary biliary cirrhosis, carnitine deficiency, carnitine palmitoyltransferase deficiency, myoadenylate deaminase deficiency, hypertriglyceridemia, lipid storage disorders such Fabry's disease, Gaucher's disease, Niemann-Pick's disease, metachromatic leukodystrophy, adrenoleukodystrophy, GM₂ gangliosidosis, and ceroid lipofuscinosis, abetalipoproteinemia, Tangier disease, hyperlipoproteinemia, lipodystrophy, lipomatoses, acute panniculitis, disseminated fat necrosis, adiposis dolorosa, lipoid adrenal hyperplasia, minimal change disease, lipomas, atherosclerosis, hypercholesterolemia, hypercholesterolemia with hypertriglyceridemia, primary hypoalphalipoproteinemia, hypothyroidism, renal disease, liver disease, lecithin:cholesterol acyltransferase deficiency, cerebrotendinous xanthomatosis, sitosterolemia, hypocholesterolemia, Tay-Sachs disease, Sandhoff's disease, hyperlipidemia, hyperlipemia, and lipid myopathies, and disorders of copper metabolism such as Menke's disease, Wilson's disease, and Ehlers-Danlos syndrome type IX diabetes; a developmental disorder such as renal tubular acidosis, anemia, Cushing's syndrome, achondroplastic dwarfism, Duchenne and Becker muscular dystrophy, epilepsy, gonadal dysgenesis, WAGR syndrome (Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation), Smith-Magenis syndrome, myelodysplastic syndrome, hereditary mucoepithelial dysplasia, hereditary keratodermas, hereditary neuropathies such as Charcot-Marie-Tooth disease and neurofibromatosis, hypothyroidism, hydrocephalus, a seizure disorder such as Syndenham's chorea and cerebral palsy, spina bifida, anencephaly, craniorachischisis, congenital glaucoma, cataract, and sensorineural hearing loss; and an endocrine disorder such as a disorder of the hypothalamus and/or pituitary resulting from lesions such as a primary brain tumor, adenoma, infarction associated with pregnancy, hypophysectomy, aneurysm, vascular malformation, thrombosis, infection, immunological disorder, and complication due to head trauma, a disorder associated with hypopituitarism including hypogonadism, Sheehan syndrome, diabetes insipidus, Kallman's disease, Hand-Schuller-Christian disease, Letterer-Siwe disease, sarcoidosis, empty sella syndrome, and dwarfism, a disorder associated with hyperpituitarism including acromegaly, giantism, and syndrome of inappropriate antidiuretic hormone (ADS) secretion (SIADH) often caused by benign adenoma, a disorder associated with hypothyroidism including goiter, myxedema, acute thyroiditis associated with bacterial infection, subacute thyroiditis associated with viral infection, autoimmune thyroiditis (Hashimoto's disease), and cretinism, a disorder associated with hyperthyroidism including thyrotoxicosis and its various forms, Grave's disease, pretibial myxedema, toxic multinodular goiter, thyroid carcinoma, and Plummer's disease, a disorder associated with hyperparathyroidism including Conn disease (chronic hypercalemia), a pancreatic disorder such as Type I or Type II diabetes mellitus and associated complications, a disorder associated with the adrenals such as hyperplasia, carcinoma, or adenoma of the adrenal cortex, hypertension associated with alkalosis, amyloidosis, hypokalemia, Cushing's disease, Liddle's syndrome, and Arnold-Healy-Gordon syndrome, pheochromocytoma tumors, and Addison's disease, a disorder associated with gonadal steroid hormones such as: in women, abnormal prolactin production, infertility, endometriosis, perturbation of the menstrual cycle, polycystic ovarian disease, hyperprolactinemia, isolated gonadotropin deficiency, amenorrhea, galactorrhea, hermaphroditism, hirsutism and virilization, breast cancer, and, in post-menopausal women, osteoporosis, and, in men, Leydig cell deficiency, male climacteric phase, and germinal cell aplasia, a hypergonadal disorder associated with Leydig cell tumors, androgen resistance associated with absence of androgen receptors, syndrome of 5 α-reductase, and gynecomastia.

[0244] In another embodiment, a vector capable of expressing REMAP or a fragment or derivative thereof may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of REMAP including, but not limited to, those described above.

[0245] In a further embodiment, a composition comprising a substantially purified REMAP in conjunction with a suitable pharmaceutical carrier may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of REMAP including, but not limited to, those provided above.

[0246] In still another embodiment, an agonist which modulates the activity of REMAP may be administered to a subject to treat or prevent a disorder associated with decreased expression or activity of REMAP including, but not limited to, those listed above.

[0247] In a further embodiment, an antagonist of REMAP maybe administered to a subject to treat or prevent a disorder associated with increased expression or activity of REMAP. Examples of such disorders include, but are not limited to, those cardiovascular, neurological, gastrointestinal, lipid metabolism, cell proliferative, autoimmune/inflammatory, metabolic, developmental, and endocrine disorders described above. In one aspect, an antibody which specifically binds REMAP may be used directly as an antagonist or indirectly as a targeting or delivery mechanism for bringing a pharmaceutical agent to cells or tissues which express REMAP.

[0248] In an additional embodiment, a vector expressing the complement of the polynucleotide encoding REMAP may be administered to a subject to treat or prevent a disorder associated with increased expression or activity of REMAP including, but not limited to, those described above.

[0249] In other embodiments, any of the proteins, antagonists, antibodies, agonists, complementary sequences, or vectors of the invention may be administered in combination with other appropriate therapeutic agents. Selection of the appropriate agents for use in combination therapy may be made by one of ordinary skill in the art, according to conventional pharmaceutical principles. The combination of therapeutic agents may act synergistically to effect the treatment or prevention of the various disorders described above. Using this approach, one may be able to achieve therapeutic efficacy with lower dosages of each agent, thus reducing the potential for adverse side effects.

[0250] An antagonist of REMAP may be produced using methods which are generally known in the art. In particular, purified REMAP may be used to produce antibodies or to screen libraries of pharmaceutical agents to identify those which specifically bind REMAP. Antibodies to REMAP may also be generated using methods that are well known in the art. Such antibodies may include, but are not limited to, polyclonal, monoclonal, chimeric, and single chain antibodies, Fab fragments, and fragments produced by a Fab expression library. Neutralzing antibodies (i.e., those which inbit dimer formation) are generally preferred for therapeutic use. Single chain antibodies (e.g., from camels or llamas) may be potent enzyme iihibitors and may have advantages in the design of peptide mimetics, and in the development of immuno-adsorbents and biosensors (Muyldermans, S. (2001) J. Biotechnol. 74:277-302).

[0251] For the production of antibodies, various hosts including goats, rabbits, rats, mice, camels, dromedaries, llamas, humans, and others may be immunized by injection with REMAP or with any fragment or oligopeptide thereof which has immunogenic properties. Depending on the host species, various adjuvants may be used to increase immunological response. Such adjuvants include, but are not limited to, Freund's, mineral gels such as aluminum hydroxide, and surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, KLH, and dinitrophenol. Among adjuvants used in humans, BCG (bacilli Calhette-Guerin) and Corynebacterium parvum are especially preferable.

[0252] It is preferred that the oligopeptides, peptides, or fragments used to induce antibodies to REMAP have an amino acid sequence consisting of at least about 5 amino acids, and generally will consist of at least about 10 amino acids. It is also preferable that these oligopeptides, peptides, or fragments are identical to a portion of the amino acid sequence of the natural protein. Short stretches of REMAP amino acids may be fused with those of another protein, such as KLH, and antibodies to the chimeric molecule may be produced.

[0253] Monoclonal antibodies to REMAP may be prepared using any technique which provides for the production of antibody molecules by continuous cell lines in culture. These include, but are not limited to, the hybridoma technique, the human B-cell hybridoma technique, and the EBV-hybridoma technique. (See, e.g., Kohler, G. et al. (1975) Nature 256:495-497; Kozbor, D. et al. (1985) J. Immunol. Methods 81:31-42; Cote, R. J. et al. (1983) Proc. Natl. Acad. Sci. USA 80:2026-2030; and Cole, S. P. et al. (1984) Mol. Cell Biol. 62:109-120.)

[0254] In addition, techniques developed for the production of “chimeric antibodies,” such as the splicing of mouse antibody genes to human antibody genes to obtain a molecule with appropriate antigen specificity and biological activity, can be used. (See, e.g., Morrison, S. L. et al. (1984) Proc. Natl. Acad. Sci. USA 81:6851-6855; Neuberger, M. S. et al. (1984) Nature 312:604-608; and Takeda, S. et al. (1985) Nature 314:452-454.) Alternatively, techniques described for the production of single chain antibodies may be adapted, using methods known in the art, to produce REMAP-specific single chain antibodies. Antibodies with related specificity, but of distinct idiotypic composition, may be generated by chain shuffling from random combinatorial immunoglobulin libraries. (See, e.g., Burton, D. R. (1991) Proc. Natl. Acad. Sci. USA 88:10134-10137.) Antibodies may also be produced by inducing in vivo production in the lymphocyte population or by screening immunoglobulin libraries or panels of highly specific binding reagents as disclosed in the literature. (See, e.g., Orlandi, R. et al. (1989) Proc. Natl. Acad. Sci. USA 86:3833-3837; Vmter, G. et al. (1991) Nature 349:293-299.)

[0255] Antibody fragments which contain specific binding sites for REMAP may also be generated. For example, such fragments include, but are not limited to, F(ab′)₂ fragments produced by pepsin digestion of the antibody molecule and Fab fragments generated by reducing the disulfide bridges of the F(ab′)2 fragments. Alternatively, Fab expression libraries may be constructed to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity. (See, e.g., Huse, W. D. et al. (1989) Science 246:1275-1281.)

[0256] Various immunoassays maybe used for screening to identity antibodies having the desired specificity. Numerous protocols for competitive binding or immunoradiometric assays using either polyclonal or monoclonal antibodies with established specificities are well known in the art. Such immunoassays typically involve the measurement of complex formation between REMAP and its specific antibody. A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering REMAP epitopes is generally used, but a competitive binding assay may also be employed (Pound, supra).

[0257] Various methods such as Scatchard analysis in conjunction with radioimmunoassay techniques may be used to assess the affinity of antibodies for REMAP. Affinity is expressed as an association constant, K_(a), which is defined as the molar concentration of REMAP-antibody complex divided by the molar concentrations of free antigen and free antibody under equilibrium conditions. The K_(a) determined for a preparation of polyclonal antibodies, which are heterogeneous in their affinities for multiple REMAP epitopes, represents the average annuity, or avidity, of the antibodies for REMAP. The K_(a) determined for a preparation of monoclonal antibodies, which are monospecific for a particular REMAP epitope, represents a true measure of affinity. High-affinity antibody preparations with K_(a) ranging from about 10⁹ to 10¹² L/mole are preferred for use in immunoassays in which the REMAP-antibody complex must withstand rigorous manipulations. Low-affinity antibody preparations with K_(a) ranging from about 10⁶ to 10⁷ L/mole are preferred for use in immunopurification and similar procedures which ultimately require dissociation of REMAP, preferably in active form, from the antibody (Catty, D. (1988) Antibodies. Volume I: A Practical Approach, IRL Press, Washington D.C.; Liddell, J. E. and A. Cryer (1991) A Practical Guide to Monoclonal Antibodies, John Wiley & Sons, New York N.Y.).

[0258] The titer and avidity of polyclonal antibody preparations may be further evaluated to determine the quality and suitability of such preparations for certain downstream applications. For example, a polyclonal antibody preparation containing at least 1-2 mg specific antibody/ml, preferably 5-10 mg specific antibody/ml is generally employed in procedures requiring precipitation of REMAP-antibody complexes. Procedures for evaluating antibody specificity, titer, and avidity, and guidelines for antibody quality and usage in various applications, are generally available. (See, e.g., Catty, supra, and Coligan et al. supra.)

[0259] In another embodiment of the invention, the polynucleotides encoding REMAP, or any fragment or complement thereof, may be used for therapeutic purposes. In one aspect, modifications of gene expression can be achieved by designing complementary sequences or antisense molecules (DNA, RNA, PNA, or modified oligonucleotides) to the coding or regulatory regions of the gene encoding REMAP. Such technology is well known in the art, and antisense oligonucleotides or larger fragments can be designed from various locations along the coding or control regions of sequences encoding REMAP. (See, e.g., Agrawal, S., ed. (1996) Antisense Therapeutics, Humana Press Inc., Totawa N.J.)

[0260] In therapeutic use, any gene delivery system suitable for introduction of the antisense sequences into appropriate target cells can be used. Antisense sequences can be delivered intracellularly in the form of an expression plasmid which, upon transcription, produces a sequence complementary to at least a portion of the cellular sequence encoding the target protein. (See, e.g., Slater, J. E. et al. (1998) J. Allergy Clin. Immunol. 102(3):469-475; and Scanlon, K. J. et al. (1995) 9(13):1288-1296.) Antisense sequences can also be introduced intracellularly through the use of viral vectors, such as retrovirus and adeno-associated virus vectors. (See, e.g., Miller, A. D. (1990) Blood 76:271; Ausubel, supra; Uckert, W. and W. Walther (1994) Pharmacol. Ther. 63(3):323-347.) Other gene delivery mechanisms include liposome-derived systems, artificial viral envelopes, and other systems known in the art. (See, e.g., Rossi, J. J. (1995) Br. Med. Bull. 51(1):217-225; Boado, R. J. et al. (1998) J. Pharm. Sci. 87(11):1308-1315; and Morris, M. C. et al. (1997) Nucleic Acids Res. 25(14):2730-2736.)

[0261] In another embodiment of the invention, polynucleotides encoding REMAP may be used for somatic or germline gene therapy. Gene therapy may be performed to (i) correct a genetic deficiency (e.g., in the cases of severe combined immunodeficiency (SCID)-X1 disease characterized by X-linked inheritance (Cavazzana-Calvo, M. et al. (2000) Science 288:669-672), severe combined immunodeficiency syndrome associated with an inherited adenosine deaminase (ADA) deficiency (Blaese, R. M. et al. (1995) Science 270:475-480; Bordignon, C. et al. (1995) Science 270:470-475), cystic fibrosis (Zabner, J. et al. (1993) Cell 75:207-216; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:643-666; Crystal, R. G. et al. (1995) Hum. Gene Therapy 6:667-703), thalassamias, familial hypercholesterolemia, and hemophilia resulting from Factor VIII or Factor IX deficiencies (Crystal, R. G. (1995) Science 270:404-410; Verma, I. M. and N. Somia (1997) Nature 389:239-242)), (ii) express a conditionally lethal gene product (e.g., in the case of cancers which result from unregulated cell proliferation), or (iii) express a protein which affords protection against intracellular parasites (e.g., against human retroviruses, such as human immunodeficiency virus (HIV) (Baltimore, D. (1988) Nature 335:395-396; Poeschla, E. et al. (1996) Proc. Natl. Acad. Sci. USA 93:11395-11399), hepatitis B or C virus (HBV, HCV); fungal parasites, such as Candida albicans and Paracoccidioides brasiliensis; and protozoan parasites such as Plasmodium falciparum and Trypanosoma cruzi). In the case where a genetic deficiency in REMAP expression or regulation causes disease, the expression of REMAP from an appropriate population of transduced cells may alleviate the clinical manifestations caused by the genetic deficiency.

[0262] In a further embodiment of the invention, diseases or disorders caused by deficiencies in REMAP are treated by constructing mammalian expression vectors encoding REMAP and introducing these vectors by mechanical means into REMAP-deficient cells. Mechanical transfer technologies for use with cells in vivo or ex vitro include (i) direct DNA microinjection into individual cells, (ii) ballistic gold particle delivery, (iii) liposome-mediated transfection, (iv) receptor-mediated gene transfer, and (v) the use of DNA transposons (Morgan, R. A. and W. F. Anderson (1993) Annu. Rev. Biochem. 62:191-217; Ivics, Z. (1997) Cell 91:501-510; Boulay, J-L. and H. Récipon (1998) Curr. Opin. Biotechnol. 9:445-450).

[0263] Expression vectors that may be effective for the expression of REMAP include, but are not limited to, the PCDNA 3.1, EPITAG, PRCCMV2, PREP, PVAX, PCR2-TOPOTA vectors (Invitrogen, Carlsbad Calif.), PCMV-SCRIPT, PCMV-TAG, PEGSH/PERV (Stratagene, La Jolla Calif.), and PTET-OFF, PTET-ON, PTRE2, PTRE2-LUC, PTK-HYG (Clontech, Palo Alto Calif.). REMAP may be expressed using (i) a constitutively active promoter, (e.g., from cytomegalovirus (CMV), Rous sarcoma virus (RSV), SV40 virus, thymidine kinase (TK), or O-actin genes), (ii) an inducible promoter (e.g., the tetracycline-regulated promoter (Gossen, M. and H. Bujard (1992) Proc. Natl. Acad. Sci. USA 89:5547-5551; Gossen, M. et al. (1995) Science 268:1766-1769; Rossi, F. M. V. and H. M. Blau (1998) Curr. Opin. Biotechnol. 9:451-456), commercially available in the T-REX plasmid (Invitrogen)); the ecdysone-inducible promoter (available in the plasmids PVGRXR and PIND; Invitrogen); the FK506/rapamycin inducible promoter; or the RU486/mifepristone inducible promoter (Rossi, F. M. V. and H. M. Blau, supra)), or (iii) a tissue-specific promoter or the native promoter of the endogenous gene encoding REMAP from a normal individual.

[0264] Commercially available liposome transformation kits (e.g., the PERFECT LIPID TRANSFECTION KIT, available from Invitrogen) allow one with ordinary skill in the art to deliver polynucleotides to target cells in culture and require minimal effort to optimize experimental parameters. In the alternative, transformation is performed using the calcium phosphate method (Graham, F. L. and A. J. Eb (1973) Virology 52:456-467), or by electroporation (Neumann, E. et al. (1982) EMBO J. 1:841-845). The introduction of DNA to primary cells requires modification of these standardized mammalian transfection protocols.

[0265] In another embodiment of the invention, diseases or disorders caused by genetic defects with respect to REMAP expression are treated by constructing a retrovirus vector consisting of (i) the polynucleotide encoding REMAP under the control of an independent promoter or the retrovirus long terminal repeat (LTR) promoter, (ii) appropriate RNA packaging signals, and (iii) a Rev-responsive element (RRE) along with additional retrovirus cis-acting RNA sequences and coding sequences required for efficient vector propagation. Retrovirus vectors (e.g., PEB and PFBNEO) are commercially available (Stratagene) and are based on published data (Riviere, I. et al. (1995) Proc. Natl. Acad. Sci. USA 92:6733-6737), incorporated by reference herein. The vector is propagated in an appropriate vector producing cell line (VPCL) that expresses an envelope gene with a tropism for receptors on the target cells or a promiscuous envelope protein such as VSVg (Armentano, D. et al. (1987) J. Virol. 61:1647-1650; Bender, M. A. et al. (1987) J. Virol. 61:1639-1646; Adam, M. A. and A. D. Miller (1988) J. Virol. 62:3802-3806; Dull, T. et al. (1998) J. Virol. 72:8463-8471; Zufferey, R. et al. (1998) J. Virol. 72:9873-9880). U.S. Pat. No. 5,910,434 to Rigg (“Method for obtaining retrovirus packaging cell lines producing high transducing efficiency retroviral supernatant”) discloses a method for obtaining retrovirus packaging cell lines and is hereby incorporated by reference. Propagation of retrovirus vectors, transduction of a population of cells (e.g., CD4⁺ T-cells), and the return of transduced cells to a patient are procedures well known to persons skilled in the art of gene therapy and have been well documented (Ranga, U. et al. (1997) J. Virol. 71:7020-7029; Bauer, G. et al. (1997) Blood 89:2259-2267; Bonyhadi, M. L. (1997) J. Virol 71:4707-4716; Ranga, U. et al. (1998) Proc. Natl. Acad. Sci. USA 95:1201-1206; Su, L. (1997) Blood 89:2283-2290).

[0266] In the alternative, an adenovirus-based gene therapy delivery system is used to deliver polynucleotides encoding REMAP to cells which have one or more genetic abnormalities with respect to the expression of REMAP. The construction and packaging of adenovirus-based vectors are well known to those with ordinary skill in the arts. Replication defective adenovirus vectors have proven to be versatile for importing genes encoding immunoregulatory proteins into intact islets in the pancreas (Csete, M. E. et al. (1995) Transplantation 27:263-268). Potentially useful adenoviral vectors are described in U.S. Pat. No. 5,707,618 to Armentano (“Adenovirus vectors for gene therapy”), hereby incorporated by reference. For adenoviral vectors, see also Antinozzi, P. A. et al. (1999) Annu. Rev. Nutr. 19:511-544 and Verma, I. M. and N. Somia (1997) Nature 18:389:239-242, both incorporated by reference herein.

[0267] In another alternative, a herpes-based, gene therapy delivery system is used to deliver polynucleotides encoding REMAP to target cells which have one or more genetic abnormalities with respect to the expression of REMAP. The use of herpes simplex virus (HSV)-based vectors may be especially valuable for introducing REMAP to cells of the central nervous system, for which HSV has a tropism The construction and packaging of herpes-based vectors are well known to those with ordinary skill in the art. A replication-competent herpes simplex virus (HSV) type 1-based vector has been used to deliver a reporter gene to the eyes of primates (Liu, X. et al. (1999) Exp. Eye Res. 169:385-395). The construction of a HSV-1 virus vector has also been disclosed in detail in U.S. Pat. No. 5,804,413 to DeLuca (“Herpes simplex virus strains for gene transfer”), which is hereby incorporated by reference. U.S. Pat. No. 5,804,413 teaches the use of recombinant HSV d92 which consists of a genome containing at least one exogenous gene to be transferred to a cell under the control of the appropriate promoter for purposes including human gene therapy. Also taught by this patent are the construction and use of recombinant HSV strains deleted for ICP4, ICP27 and ICP22. For HSV vectors, see also Goins, W. F. et al. (1999) J. Virol. 73:519-532 and Xu, H. et al. (1994) Dev. Biol. 163:152-161, hereby incorporated by reference. The manipulation of cloned herpesvirus sequences, the generation of recombinant virus following the transfection of multiple plasmids containing different segments of the large herpesvirus genomes, the growth and propagation of herpesvirus, and the infection of cells with herpesvirus are techniques well known to those of ordinary skill in the art.

[0268] In another alternative, an alphavirus (positive, single-stranded RNA virus) vector is used to deliver polynucleotides encoding REMAP to target cells. The biology of the prototypic alphavirus, Semliki Porest Virus (SFV), has been studied extensively and gene transfer vectors have been based on the SPV genome (Garoff, H. and K.-J. Li (1998) Curr. Opin. Biotechnol. 9:464-469). During alphavirus RNA replication, a subgenomic RNA is generated that normally encodes the viral capsid proteins. This subgenomic RNA replicates to higher levels than the full length genomic RNA, resulting in the overproduction of capsid proteins relative to the viral proteins with enzymatic activity (e.g., protease and polymerase). Similarly, inserting the coding sequence for REMAP into the alphavirus genome in place of the capsid-coding region results in the production of a large number of REMAP-coding RNAs and the synthesis of high levels of REMAP in vector transduced cells. While alphavirus infection is typically associated with cell lysis within a few days, the ability to establish a persistent infection in hamster normal kidney cells (BHK-21) with a variant of Sindbis virus (SIN) indicates that the lytic replication of alphaviruses can be altered to suit the needs of the gene therapy application (Dryga, S. A. et al. (1997) Virology 228:74-83). The wide host range of alphaviruses will allow the introduction of REMAP into a variety of cell types. The specific transduction of a subset of cells in a population may require the sorting of cells prior to transduction. The methods of manipulating infectious cDNA clones of alphaviruses, performing alphavirus cDNA and RNA transfections, and performing alphavirns infections, are well known to those with ordinary skill in the art.

[0269] Oligonucleotides derived from the transcription initiation site, e.g., between about positions −10 and +10 from the start site, may also be employed to inhibt gene expression. Similarly, inhibition can be achieved using triple helix base-pairing methodology. Triple helix pairing is useful because it causes inhibition of the ability of the double helix to open sufficiently for the binding of polymerase, transcription factors, or regulatory molecules. Recent therapeutic advances using triplex DNA have been described in the literature. (See, e.g., Gee, J. E. et al. (1994) in Huber, B. E. and B. I. Carr, Molecular and Immunologic Approaches, Putura Publishing, Mt. Kisco N.Y., pp. 163-177.) A complementary sequence or antisense molecule may also be designed to block translation of mRNA by preventing the transcript from binding to ribosomes.

[0270] Ribozymes, enzymatic RNA molecules, may also be used to catalyze the specific cleavage of RNA. The mechanism of ribozyme action involves sequence-specific hybridization of the ribozyme molecule to complementary target RNA, followed by endonucleolytic cleavage. For example, engineered hammerhead motif ribozyme molecules may specifically and efficiently catalyze endonucleolytic cleavage of sequences encoding REMAP.

[0271] Specific ribozyme cleavage sites within any potential RNA target are initially identified by scanning the target molecule for ribozyme cleavage sites, including the following sequences: GUA, GUU, and GUC. Once identified, short RNA sequences of between 15 and 20 ribonucleotides, corresponding to the region of the target gene containing the cleavage site, may be evaluated for secondary structural features which may render the oligonucleotide inoperable. The suitability of candidate targets may also be evaluated by testing accessibility to hybridization with complementary oligonucleotides using ribonuclease protection assays.

[0272] Complementary ribonucleic acid molecules and ribozymes of the invention may be prepared by any method known in the art for the synthesis of nucleic acid molecules. These include techniques for chemically synthesizing oligonucleotides such as solid phase phosphoramidite chemical synthesis. Alternatively, RNA molecules may be generated by in vitro and in vivo transcription of DNA sequences encoding REMAP. Such DNA sequences may be incorporated into a wide variety of vectors with suitable RNA polymerase promoters such as T7 or SP6. Alternatively, these cDNA constructs that synthesize complementary RNA, constitutively or inducibly, can be introduced into cell lines, cells, or tissues.

[0273] RNA molecules may be modified to increase intracellular stability and half-life. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends of the molecule, or the use of phosphorothioate or 2′O-methyl rather than phosphodiesterase linkages within the backbone of the molecule. This concept is inherent in the production of PNAs and can be extended in all of these molecules by the inclusion of nontraditional bases such as inosine, queosine, and wybutosine, as well as acetyl-, methyl-, thio-, and similarly modified forms of adenine, cytidine, guanine, thymine, and uridine which are not as easily recognized by endogenous endonucleases.

[0274] An additional embodiment of the invention encompasses a method for screening for a compound which is effective in altering expression of a polynucleotide encoding REMAP. Compounds which may be effective in altering expression of a specific polynucleotide may include, but are not limited to, oligonucleotides, antisense oligonucleotides, triple helix-forming oligonucleotides, transcription factors and other polypeptide transcriptional regulators, and non-macromolecular chemical entities which are capable of interacting with specific polynucleotide sequences. Effective compounds may alter polynucleotide expression by acting as either inhibitors or promoters of polynucleotide expression. Thus, in the treatment of disorders associated with increased REMAP expression or activity, a compound which specifically inhibits expression of the polynucleotide encoding REMAP may be therapeutically useful, and in the treatment of disorders associated with decreased REMAP expression or activity, a compound which specifically promotes expression of the polynucleotide encoding REMAP may be therapeutically useful.

[0275] At least one, and up to a plurality, of test compounds may be screened for effectiveness in altering expression of a specific polynucleotide. A test compound may be obtained by any method commonly known in the art, including chemical modification of a compound known to be effective in altering polynucleotide expression; selection from an existing, commercially-available or proprietary library of naturally-occurring or non-natural chemical compounds; rational design of a compound based on chemical and/or structural properties of the target polynucleotide; and selection from a library of chemical compounds created combinatorially or randomly. A sample comprising a polynucleotide encoding REMAP is exposed to at least one test compound thus obtained. The sample may comprise, for example, an intact or permeabilized cell, or an in vitro cell-free or reconstituted biochemical system. Alterations in the expression of a polynucleotide encoding REMAP are assayed by any method commonly known in the art. Typically, the expression of a specific nucleotide is detected by hybridization with a probe having a nucleotide sequence complementary to the sequence of the polynucleotide encoding REMAP. The amount of hybridization may be quantified, thus forming the basis for a comparison of the expression of the polynucleotide both with and without exposure to one or more test compounds. Detection of a change in the expression of a polynucleotide exposed to a test compound indicates that the test compound is effective in altering the expression of the polynucleotide. A screen for a compound effective in altering expression of a specific polynucleotide can be carried out, for example, using a Schizosaccharomyces pombe gene expression system (Atkins, D. et al. (1999) U.S. Pat. No. 5,932,435; Arndt, G. M. et al. (2000) Nucleic Acids Res. 28:E15) or a human cell line such as HeLa cell (Clarke, M. L. et al. (2000) Biochem. Biophys. Res. Commun. 268:8-13). A particular embodiment of the present invention involves screening a combinatorial library of oligonucleotides (such as deoxyribonucleotides, ribonucleotides, peptide nucleic acids, and modified oligonucleotides) for antisense activity against a specific polynucleotide sequence (Bruice, T. W. et al. (1997) U.S. Pat. No. 5,686,242; Bruice, T. W. et al. (2000) U.S. Pat. No. 6,022,691).

[0276] Many methods for introducing vectors into cells or tissues are available and equally suitable for use in vivo, in vitro, and ex vivo. For ex vivo therapy, vectors maybe introduced into stem cells taken from the patient and clonally propagated for autologous transplant back into that same patient. Delivery by transfection, by liposome injections, or by polycationic amino polymers may be achieved using methods which are well known in the art. (See, e.g., Goldman, C. K. et al. (1997) Nat Biotechnol. 15:462-466.)

[0277] Any of the therapeutic methods described above may be applied to any subject in need of such therapy, including, for example, mammals such as humans, dogs, cats, cows, horses, rabbits, and monkeys.

[0278] An additional embodiment of the invention relates to the administration of a composition which generally comprises an active ingredient formulated with a pharmaceutically acceptable excipient. Excipients may include, for example, sugars, starches, celluloses, gums, and proteins. Various formulations are commonly known and are thoroughly discussed in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing, Easton Pa.). Such compositions may consist of REMAP, antibodies to REMAP, and mimetics, agonists, antagonists, or inhibitors of REMAP.

[0279] The compositions utilized in this invention may be administered by any number of routes including, but not limited to, oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, pulmonary, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal means.

[0280] Compositions for pulmonary administration may be prepared in liquid or dry powder form These compositions are generally aerosolized immediately prior to inhalation by the patient. In the case of small molecules (e.g. traditional low molecular weight organic drugs), aerosol delivery of fast-acting formulations is well-known in the art. In the case of macromolecules (e.g. larger peptides and proteins), recent developments in the field of pulmonary delivery via the alveolar region of the lung have enabled the practical delivery of drugs such as insulin to blood circulation (see, e.g., Patton, J. S. et al., U.S. Pat. No. 5,997,848). Pulmonary delivery has the advantage of administration without needle injection, and obviates the need for potentially toxic penetration enhancers.

[0281] Compositions suitable for use in the invention include compositions wherein the active ingredients are contained in an effective amount to achieve the intended purpose. The determination of an effective dose is well within the capability of those skilled in the art.

[0282] Specialized forms of compositions may be prepared for direct intracellular delivery of macromolecules comprising REMAP or fragments thereof. For example, liposome preparations containing a cell-impermeable macromolecule may promote cell fusion and intracellular delivery of the macromolecule. Alternatively, REMAP or a fragment thereof may be joined to a short cationic N-terminal portion from the HIV Tat-1 protein. Fusion proteins thus generated have been found to transduce into the cells of all tissues, including the brain, in a mouse model system (Schwarze, S. R. et al. (1999) Science 285:1569-1572).

[0283] For any compound, the therapeutically effective dose can be estimated initially either in cell culture assays, e.g., of neoplastic cells, or in animal models such as mice, rats, rabbits, dogs, monkeys, or pigs. An animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans.

[0284] A therapeutically effective dose refers to that amount of active ingredient, for example REMAP or fragments thereof, antibodies of REMAP, and agonists, antagonists or inhibitors of REMAP, which ameliorates the symptoms or condition. Therapeutic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or with experimental animals, such as by calculating the ED₅₀ (the dose therapeutically effective in 50% of the population) or LD50 (the dose lethal to 50% of the population) statistics. The dose ratio of toxic to therapeutic effects is the therapeutic index, which can be expressed as the LD₅₀/ED₅₀ ratio. Compositions which exhibit large therapeutic indices are preferred. The data obtained from cell culture assays and animal studies are used to formulate a range of dosage for human use. The dosage contained in such compositions is preferably within a range of circulating concentrations that includes the ED₅₀ with little or no toxicity. The dosage varies within this range depending upon the dosage form employed, the sensitivity of the patient, and the route of administration.

[0285] The exact dosage will be determined by the practitioner, in light of factors related to the subject requiring treatment. Dosage and administration are adjusted to provide sufficient levels of the active moiety or to maintain the desired effect. Factors which may be taken into account include the severity of the disease state, the general health of the subject, the age, weight, and gender of the subject, time and frequency of administration, drug combination(s), reaction sensitivities, and response to therapy. Long-acting compositions may be administered every 3 to 4 days, every week, or biweekly depending on the half-life and clearance rate of the particular formulation.

[0286] Normal dosage amounts may vary from about 0.1 μg to 100,000 μg, up to a total dose of about 1 gram, depending upon the route of administration. Guidance as to particular dosages and methods of delivery is provided in the literature and generally available to practitioners in the art. Those skilled in the art will employ different formulations for nucleotides than for proteins or their inhibitors. Similarly, delivery of polynucleotides or polypeptides will be specific to particular cells, conditions, locations, etc.

[0287] Diagnostics

[0288] In another embodiment, antibodies which specifically bind REMAP maybe used for the diagnosis of disorders characterized by expression of REMAP, or in assays to monitor patients being treated with REMAP or agonists, antagonists, or inhibitors of REMAP. Antibodies useful for diagnostic purposes may be prepared in the same manner as described above for therapeutics. Diagnostic assays for REMAP include methods which utilize the antibody and a label to detect REMAP in human body fluids or in extracts of cells or tissues. The antibodies may be used with or without modification, and may be labeled by covalent or non-covalent attachment of a reporter molecule. A wide variety of reporter molecules, several of which are described above, are known in the art and may be used.

[0289] A variety of protocols for measuring REMAP, including ELISAs, RIAs, and FACS, are known in the art and provide a basis for diagnosing altered or abnormal levels of REMAP expression. Normal or standard values for REMAP expression are established by combining body fluids or cell extracts taken from normal mammalian subjects, for example, human subjects, with antibodies to REMAP under conditions suitable for complex formation. The amount of standard complex formation may be quantitated by various methods, such as photometric means. Quantities of REMAP expressed in subject, control, and disease samples from biopsied tissues are compared with the standard values. Deviation between standard and subject values establishes the parameters for diagnosing disease.

[0290] In another embodiment of the invention, the polynucleotides encoding REMAP may be used for diagnostic purposes. The polynucleotides which may be used include oligonucleotide sequences, complementary RNA and DNA molecules, and PNAs. The polynucleotides may be used to detect and quantify gene expression in biopsied tissues in which expression of REMAP maybe correlated with disease. The diagnostic assay maybe used to determine absence, presence, and excess expression of REMAP, and to monitor regulation of REMAP levels during therapeutic intervention.

[0291] In one aspect, hybridization with PCR probes which are capable of detecting polynucleotide sequences, including genomic sequences, encoding REMAP or closely related molecules maybe used to identify nucleic acid sequences which encode REMAP. The specificity of the probe, whether it is made from a highly specific region, e.g., the 5′ regulatory region, or from a less specific region, e.g., a conserved motif, and the stringency of the hybridization or amplification will determine whether the probe identifies only naturally occurring sequences encoding REMAP, allelic variants, or related sequences.

[0292] Probes may also be used for the detection of related sequences, and may have at least 50% sequence identity to any of the REMAP encoding sequences. The hybridization probes of the subject invention may be DNA or RNA and maybe derived from the sequence of SEQ ID NO:44-86 or from genomic sequences including promoters, enhancers, and introns of the REMAP gene.

[0293] Means for producing specific hybridization probes for DNAs encoding REMAP include the cloning of polynucleotide sequences encoding REMAP or REMAP derivatives into vectors for the production of mRNA probes. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by means of the addition of the appropriate RNA polymerases and the appropriate labeled nucleotides. Hybridization probes maybe labeled by a variety of reporter groups, for example, by radionuclides such as ³²P or ³⁵S, or by enzymatic labels, such as alkaline phosphatase coupled to the probe via avidin/biotin coupling systems, and the like.

[0294] Polynucleotide sequences encoding REMAP may be used for the diagnosis of disorders associated with expression of REMAP. Examples of such disorders include, but are not limited to, a cardiovascular disorder including blood vessel disorders such as arteriovenous fistula, atherosclerosis, hypertension, vasculitis, Raynaud's disease, aneurysms, arterial dissections, varicose veins, thrombophlebitis and phlebothrombosis, vascular tumors, and complications of thrombolysis, balloon angioplasty, vascular replacement, and coronary artery bypass graft surgery, heart disorders such as congestive heart failure, ischemic heart disease, angina pectoris, myocardial infarction, hypertensive heart disease, degenerative valvular heart disease, calcific aortic valve stenosis, congenitally bicuspid aortic valve, mitral annular calcification, mitral valve prolapse, rheumatic fever and rheumatic heart disease, infective endocarditis, nonbacterial thrombotic endocarditis, endocarditis of systemic lupus erythematosus, carcinoid heart disease, cardiomyopathy, myocarditis, pericarditis, neoplastic heart disease, congenital heart disease, and complications of cardiac transplantation, and lung disorders such as congenital lung anomalies, atelectasis, pulmonary congestion and edema, pulmonary embolism, pulmonary hemorrhage, pulmonary infarction, pulmonary hypertension, vascular sclerosis, obstructive pulmonary disease, restrictive pulmonary disease, chronic obstructive pulmonary disease, emphysema, chronic bronchitis, bronchial asthma, bronchiectasis, bacterial pneumonia, viral and mycoplasmal pneumonia, lung abscess, pulmonary tuberculosis, diffuse interstitial diseases, pneumoconioses, sarcoidosis, idiopathic pulmonary fibrosis, desquamative interstitial pneumonitis, hypersensitivity pneumonitis, pulmonary eosinophilia bronchiolitis obliterans-organizing pneumonia, diffuse pulmonary hemorrhage syndromes, Goodpasture's syndromes, idiopathic pulmonary hemosiderosis, pulmonary involvement in collagen-vascular disorders, pulmonary alveolar proteinosis, lung tumors, inflammatory and noninflammatory pleural effusions, pneumothorax, pleural tumors, drug-induced lung disease, radiation-induced lung disease, and complications of lung transplantation; a neurological disorder such as epilepsy, ischemic cerebrovascular disease, stroke, cerebral neoplasms, Alzeimer's disease, Pick's disease, Huntington's disease, dementia, Parkinson's disease and other extrapyramidal disorders, amyotrophic lateral sclerosis and other motor neuron disorders, progressive neural muscular atrophy, retinitis pigmentosa, hereditary ataxias, multiple sclerosis and other demyelinating diseases, bacterial and viral meningitis, brain abscess, subdural empyema, epidural abscess, suppurative intracranial thrombophlebitis, myelitis and radiculitis, viral central nervous system disease, prion diseases including kuru, Creutzfeldt-Jakob disease, and Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia, nutritional and metabolic diseases of the nervous system, neurofibromatosis, tuberous sclerosis, cerebelloretinal hemangioblastomatosis, encephalotrigeminal syndrome, mental retardation and other developmental disorders of the central nervous system, cerebral palsy, neuroskeletal disorders, autonomic nervous system disorders, cranial nerve disorders, spinal cord diseases, muscular dystrophy and other neuromuscular disorders, peripheral nervous system disorders, dermatomyositis and polymyositis, inherited, metabolic, endocrine, and toxic myopathies, myasthenia gravis, periodic paralysis, mental disorders including mood, anxiety, and schizophrenic disorders, seasonal affective disorder (SAD), akathesia, amnesia, catatonia, diabetic neuropathy, tardive dyskinesia, dystonias, paranoid psychoses, postherpetic neuralgia, Tourette's disorder, progressive supranuclear palsy, corticobasal degeneration, and familial frontotemporal dementia; a gastrointestinal disorder such as dysphagia, peptic esophagitis, esophageal spasm, esophageal stricture, esophageal carcinoma, dyspepsia, indigestion, gastritis, gastric carcinoma, anorexia, nausea, emesis, gastroparesis, antral or pyloric edema, abdominal angina, pyrosis, gastroenteritis, intestinal obstruction, infections of the intestinal tract, peptic ulcer, cholelithiasis, cholecystitis, cholestasis, pancreatitis, pancreatic carcinoma, biliary tract disease, hepatitis, hyperbilinibinemia, cirrhosis, passive congestion of the liver, hepatoma, infectious colitis, ulcerative colitis, ulcerative proctitis, Crohn's disease, Whipple's disease, Mallory-Weiss syndrome, colonic carcinoma, colonic obstruction, irritable bowel syndrome, short bowel syndrome, diarrhea, constipation, gastrointestinal hemorrhage, acquired immunodeficiency syndrome (AIDS) enteropathy, jaundice, hepatic encephalopathy, hepatorenal syndrome, hepatic steatosis, hemochromatosis, Wilson's disease, alpha₁-antitrypsin deficiency, Reye's syndrome, primary sclerosing cholangitis, liver infarction, portal vein obstruction and thrombosis, centrilobular necrosis, peliosis hepatis, hepatic vein thrombosis, veno-occlusive disease, preeclampsia, eclampsia, acute fatty liver of pregnancy, intrahepatic cholestasis of pregnancy, and hepatic tumors including nodular hyperplasias, adenomas, and carcinomas; a disorder of lipid metabolism such as fatty liver, cholestasis, primary biliary cirrhosis, carnitine deficiency, carnitine palmitoyltransferase deficiency, myoadenylate deaminase deficiency, hypertriglyceridemia, lipid storage disorders such Fabry's disease, Gaucher's disease, Niemann-Pick's disease, metachromatic leukodystrophy, adrenoleukodystrophy, GM2 gangliosidosis, and ceroid lipofuscinosis, abetalipoproteinemia, Tangier disease, hyperlipoproteinemia, diabetes mellitus, lipodystrophy, lipomatoses, acute panniculitis, disseminated fat necrosis, adiposis dolorosa, lipoid adrenal hyperplasia, minimal change disease, lipomas, atherosclerosis, hypercholesterolemia, hypercholesterolemia with hypertriglyceridemia, primary hypoalphalipoproteinemia, hypothyroidism, renal disease, liver disease, lecithin:cholesterol acyltransferase deficiency, cerebrotendinous xanthomatosis, sitosterolemia, hypocholesterolemia, Tay-Sachs disease, Sandhoff's disease, hyperlipidemia, hyperlipemia, lipid myopathies, and obesity; a cell proliferative disorder such as actinic keratosis, arteriosclerosis, atherosclerosis, bursitis, cirrhosis, hepatitis, mixed connective tissue disease (MCD), myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythemia vera, psoriasis, primary thrombocythemia, and cancers including adenocarcinoma, leukemia, lymphoma, melanoma, myeloma, sarcoma, teratocarcinoma, and, in particular, cancers of the adrenal gland, bladder, bone, bone marrow, brain, breast, cervix, gall bladder, ganglia, gastrointestinal tract, heart, kidney, liver, lung, muscle, ovary, pancreas, parathyroid, penis, prostate, salivary glands, skin, spleen, testis, thymus, thyroid, and uterus; an autoimmune/inflammatory disorder such as acquired immunodeficiency syndrome (AIDS), Addison's disease, adult respiratory distress syndrome, ankylosing spondylitis, amyloidosis, anemia, asthma, atherosclerosis, autoimmune hemolytic anemia, autoimmune thyroiditis, autoimmune polyenodocrinopathy-candidiasis-ectodermal dystrophy (APECED), bronchitis, cholecystitis, contact dermatitis, Crohn's disease, atopic dermatitis, dermatomyositis, diabetes mellitus, emphysema, episodic lymphopenia with lymphocytotoxins, erydiroblastosis fetalis, erythema nodosum, atrophic gastritis, glomerulonephritis, Goodpasture's syndrome, gout, Graves' disease, Hashimoto's thyroiditis, hypereosinophilia, irritable bowel syndrome, multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, osteoarihritis, osteoporosis, pancreatitis, polymyositis, psoriasis, Reiter's syndrome, rheumatoid arthritis, scleroderma, Sjögren's syndrome, systemic anaphylaxis, systemic lupus erythematosus, systemic sclerosis, thrombocytopenic purpura, ulcerative colitis, uveitis, Werner syndrome, complications of cancer, hemodialysis, and extracorporeal circulation, viral, bacterial, fungal, parasitic, protozoal, and helminthic infections, and trauma; a metabolic disorder such as Addison's disease, cerebrotendinous xanthomatosis, congenital adrenal hyperplasia, coumarin resistance, cystic fibrosis, fatty hepatocirrhosis, fructose-1,6-diphosphatase deficiency, galactosemia, goiter, glucagonoma, glycogen storage diseases, hereditary fructose intolerance, hyperadrenalism, hypoadrenalisr, hyperparathyroidism, hypoparathyroidism, hypercholesterolemia, hyperthyroidism, hypoglycemia, hypothyroidism, hyperlipidemia, hyperlipemia, lipid myopathies, lipodystrophies, lysosomal storage diseases, mannosidosis, neuraminidase deficiency, obesity, osteoporosis, phenylketonuria, pseudovitamin D-deficiency rickets, disorders of carbohydrate metabolism such as congenital type II dyserythropoietic anemia, diabetes, insulin-dependent diabetes mellitus, non-insulin-dependent diabetes mellitus, galactose epimerase deficiency, glycogen storage diseases, lysosomal storage diseases, fructosuria, pentosuria, and inherited abnormalities of pyruvate metabolism, disorders of lipid metabolism such as fatty liver, cholestasis, primary biliary cirrhosis, carnitine deficiency, carnitine palmitoyltransferase deficiency, myoadenylate deaminase deficiency, hypertriglyceridemia, lipid storage disorders such Fabry's disease, Gaucher's disease, Niemann-Pick's disease, metachromatic leukodystrophy, adrenoleukodystrophy, GM₂ gangliosidosis, and ceroid lipofuscinosis, abetauipoproteinemia, Tangier disease, hyperlipoproteinemia, lipodystrophy, lipomatoses, acute panniculitis, disseminated fat necrosis, adiposis dolorosa, lipoid adrenal hyperplasia, minimal change disease, lipomas, atherosclerosis, hypercholesterolemia, hypercholesterolemia with hypertriglyceridemia, primary hypoalphalipoproteinemia, hypothyroidism, renal disease, liver disease, lecithin:cholesterol acyltransferase deficiency, cerebrotendinous xanthomatosis, sitosterolemia, hypocholesterolemia, Tay-Sachs disease, Sandhoff's disease, hyperlipidemia, hyperlipemia, and lipid myopathies, and disorders of copper metabolism such as Menke's disease, Wilson's disease, and Eblers-Danlos syndrome type IX diabetes; a developmental disorder such as renal tubular acidosis, anemia, Cushing's syndrome, achondroplastic dwarfism, Duchenne and Becker muscular dystrophy, epilepsy, gonadal dysgenesis, WAGR syndrome (Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation), Smith-Magenis syndrome, myelodysplastic syndrome, hereditary mucoepithelial dysplasia, hereditary keratodermas, hereditary neuropathies such as Charcot-Marie-Tooth disease and neurofibromatosis, hypothyroidism, hydrocephalus, a seizure disorder such as Syndenham's chorea and cerebral palsy, spina bifida, anencephaly, craniorachischisis, congenital glaucoma, cataract, and sensorineural hearing loss; and an endocrine disorder such as a disorder of the hypothalamus and/or pituitary resulting from lesions such as a primary brain tumor, adenoma, infarction associated with pregnancy, hypophysectomy, aneurysm, vascular malformation, thrombosis, infection, immunological disorder, and complication due to head trauma, a disorder associated with hypopituitarism including hypogonadism, Sheehan syndrome, diabetes insipidus, Kallman's disease, Hand-Schuller-Christian disease, Letterer-Siwe disease, sarcoidosis, empty sella syndrome, and dwarfism, a disorder associated with hyperpituitarism including acromegaly, giantism, and syndrome of inappropriate antidiuretic hormone (ADH) secretion (SIADH) often caused by benign adenoma, a disorder associated with hypothyroidism including goiter, myxedema, acute thyroiditis associated with bacterial infection, subacute thyroiditis associated with viral infection, autoimmune thyroiditis (Hashiimoto's disease), and cretinism, a disorder associated with hyperhyroidism including thyrotoxicosis and its various forms, Grave's disease, pretibial myxedema, toxic multimodular goiter, thyroid carcinoma, and Plummer's disease, a disorder associated with hyperparathyroidism including Conn disease (chronic hypercalemia), a pancreatic disorder such as Type I or Type II diabetes mellitus and associated complications, a disorder associated with the adrenals such as hyperplasia, carcinoma, or adenoma of the adrenal cortex, hypertension associated with alkalosis, amyloidosis, hypokalemia, Cushing's disease, Liddle's syndrome, and Arnold-Healy-Gordon syndrome, pheochromocytoma tumors, and Addison's disease, a disorder associated with gonadal steroid hormones such as: in women, abnormal prolactin production, infertility, endometriosis, perturbation of the menstrual cycle, polycystic ovarian disease, hyperprolactinemia, isolated gonadotropin deficiency, amenorrhea, galactorthea, hermaphroditism, hirsutism and virilization, breast cancer, and, in post-menopausal women, osteoporosis, and, in men, Leydig cell deficiency, male climacteric phase, and germinal cell aplasia, a hypergonadal disorder associated with Leydig cell tumors, androgen resistance associated with absence of androgen receptors, syndrome of 5 α-reductase, and gynecomastia. The polynucleotide sequences encoding REMAP may be used in Southern or northern analysis, dot blot, or other membrane-based technologies; in PCR technologies; in dipstick, pin, and multiformat ELISA-like assays; and in microarrays utlizing fluids or tissues from patients to detect altered REMAP expression. Such qualitative or quantitative methods are well known in the art.

[0295] In a particular aspect, the nucleotide sequences encoding REMAP may be useful in assays that detect the presence of associated disorders, particularly those mentioned above. The nucleotide sequences encoding REMAP may be labeled by standard methods and added to a fluid or tissue sample from a patient under conditions suitable for the formation of hybridization complexes. After a suitable incubation period, the sample is washed and the signal is quantified and compared with a standard value. If the amount of signal in the patient sample is significantly altered in comparison to a control sample then the presence of altered levels of nucleotide sequences encoding REMAP in the sample indicates the presence of the associated disorder. Such assays may also be used to evaluate the efficacy of a particular therapeutic treatment regimen in animal studies, in clinical trials, or to monitor the treatment of an individual patient.

[0296] In order to provide a basis for the diagnosis of a disorder associated with expression of REMAP, a normal or standard profile for expression is established. This may be accomplished by combining body fluids or cell extracts taken from normal subjects, either animal or human, with a sequence, or a fragment thereof, encoding REMAP, under conditions suitable for hybridization or amplification. Standard hybridization may be quantified by comparing the values obtained from normal subjects with values from an experiment in which a known amount of a substantially purified polynucleotide is used. Standard values obtained in this manner may be compared with values obtained from samples from patients who are symptomatic for a disorder. Deviation from standard values is used to establish the presence of a disorder.

[0297] Once the presence of a disorder is established and a treatment protocol is initiated, hybridization assays may be repeated on a regular basis to determine if the level of expression in the patient begins to approximate that which is observed in the normal subject. The results obtained from successive assays may be used to show the efficacy of treatment over a period ranging from several days to months.

[0298] With respect to cancer, the presence of an abnormal amount of transcript (either under- or overexpressed) in biopsied tissue from an individual may indicate a predisposition for the development of the disease, or may provide a means for detecting the disease prior to the appearance of actual clinical symptoms. A more definitive diagnosis of this type may allow health professionals to employ preventative measures or aggressive treatment earlier thereby preventing the development or further progression of the cancer.

[0299] Additional diagnostic uses for oligonucleotides designed from the sequences encoding REMAP may involve the use of PCR. These oligomers may be chemically synthesized, generated enzymatically, or produced in vitro. Oligomers will preferably contain a fragment of a polynucleotide encoding REMAP, or a fragment of a polynucleotide complementary to the polynucleotide encoding REMAP, and will be employed under optimizd conditions for identification of a specific gene or condition. Oligomers may also be employed under less stringent conditions for detection or quantification of closely related DNA or RNA sequences.

[0300] In a particular aspect, oligonucleotide primers derived from the polynucleotide sequences encoding REMAP may be used to detect single nucleotide polymorphisms (SNPs). SNPs are substitutions, insertions and deletions that are a frequent cause of inherited or acquired genetic disease in humans. Methods of SNP detection include, but are not limited to, single-stranded conformation polymorphism (SSCP) and fluorescent SSCP (fSSCP) methods. In SSCP, oligonucleotide primers derived from the polynucleotide sequences encoding REMAP are used to amplify DNA using the polymerase chain reaction (PCR). The DNA may be derived, for example, from diseased or normal tissue, biopsy samples, bodily fluids, and the like. SNPs in the DNA cause differences in the secondary and tertiary structures of PCR products in single-stranded form, and these differences are detectable using gel electrophoresis in non-denaturing gels. In fSCCP, the oligonucleotide primers are fluorescently labeled, which allows detection of the amplimers in high-throughput equipment such as DNA sequencing machines. Additionally, sequence database analysis methods, termed in silico SNP (isSNP), are capable of identifying polymorphisms by comparing the sequence of individual overlapping DNA fragments which assemble into a common consensus sequence. These computer-based methods filter out sequence variations due to laboratory preparation of DNA and sequencing errors using statistical models and automated analyses of DNA sequence chromatograms. In the alternative, SNPs may be detected and characterized by mass spectrometry using, for example, the high throughput MASSARRAY system (Sequenom, Inc., San Diego Calif.).

[0301] SNPs may be used to study the genetic basis of human disease. For example, at least 16 common SNPs have been associated with non-insulin-dependent diabetes mellitus. SNPs are also useful for examining differences in disease outcomes in monogenic disorders, such as cystic fibrosis, sickle cell anemia, or chronic granulomatous disease. For example, variants in the mannose-binding lectin, MBL2, have been shown to be correlated with deleterious pulmonary outcomes in cystic fibrosis. SNPs also have utility in pharmacogenomics, the identification of genetic variants that influence a patient's response to a drug, such as life-threatening toxicity. For example, a variation in N-acetyl transferase is associated with a high incidence of peripheral neuropathy in response to the anti-tuberculosis drug isoniazid, while a variation in the core promoter of the ALOX5 gene results in diminished clinical response to treatment with an anti-asthma drug that targets the 5-lipoxygenase pathway. Analysis of the distribution of SNPs in different populations is useful for investigating genetic drift, mutation, recombination, and selection, as well as for tracing the origins of populations and their migrations. (Taylor, J. G. et al. (2001) Trends Mol. Med. 7:507-512; Kwok, P.-Y. and Z. Gu (1999) Mol. Med. Today 5:538-543; Nowotny, P. et al. (2001) Curr. Opin. Neurobiol. 11:637-641.)

[0302] Methods which may also be used to quantify the expression of REMAP include radiolabeling or biotinylating nucleotides, coamplification of a control nucleic acid, and interpolating results from standard curves. (See, e.g., Melby, P. C. et al. (1993) J. Immunol Methods 159:235-244; Duplaa, C. et al (1993) Anal. Biochem. 212:229-236.) The speed of quantitation of multiple samples maybe accelerated by running the assay in a high-throughput format where the oligomer or polynucleotide of interest is presented in various dilutions and a spectrophotometric or colorimetric response gives rapid quantitation.

[0303] In further embodiments, oligonucleotides or longer fragments derived from any of the polynucleotide sequences described herein may be used as elements on a microarray. The microarray can be used in transcript imaging techniques which monitor the relative expression levels of large numbers of genes simultaneously as described below. The microarray may also be used to identify genetic variants, mutations, and polymorphisms. This information may be used to determine gene function, to understand the genetic basis of a disorder, to diagnose a disorder, to monitor progression/regression of disease as a function of gene expression, and to develop and monitor the activities of therapeutic agents in the treatment of disease. In particular, this information maybe used to develop a pharmacogenomic profile of a patient in order to select the most appropriate and effective treatment regimen for that patient. For example, therapeutic agents which are highly effective and display the fewest side effects maybe selected for a patient based on his/her pharmacogenomic profile.

[0304] In another embodiment, REMAP, fragments of REMAP, or antibodies specific for REMAP may be used as elements on a microarray. The microarray may be used to monitor or measure protein-protein interactions, drug-target interactions, and gene expression profiles, as described above.

[0305] A particular embodiment relates to the use of the polynucleotides of the present invention to generate a transcript image of a tissue or cell type. A transcript image represents the global pattern of gene expression by a particular tissue or cell type. Global gene expression patterns are analyzed by quantifying the number of expressed genes and their relative abundance under given conditions and at a given time. (See Sejihamer et al., “Comparative Gene Transcript Analysis,” U.S. Pat. No. 5,840,4847 expressly incorporated by reference herein.) Thus a transcript image maybe generated by hybridizing the polynucleotides of the present invention or their complements to the totality of transcripts or reverse transcripts of a particular tissue or cell type. In one embodiment, the hybridization takes place in high-throughput format, wherein the polynucleotides of the present invention or their complements comprise a subset of a plurality of elements on a microarray. The resultant transcript image would provide a profile of gene activity.

[0306] Transcript images may be generated using transcripts isolated from tissues, cell lines, biopsies, or other biological samples. The transcript image may thus reflect gene expression in vivo, as in the case of a tissue or biopsy sample, or in vitro, as in the case of a cell line.

[0307] Transcript images which profile the expression of the polynucleotides of the present invention may also be used in conjunction with in vitro model systems and preclinical evaluation of pharmaceuticals, as well as toxicological testing of industrial and naturally-occurring environmental compounds. All compounds induce characteristic gene expression patterns, frequently termed molecular fingerprints or toxicant signatures, which are indicative of mechanisms of action and toxicity (Nuwaysir, E. F. et al. (1999) Mol. Carcinog. 24:153-159; Steiner, S. and N. L. Anderson (2000) Toxicol. Lett. 112-113:467-471, expressly incorporated by reference herein). If a test compound has a signature similar to that of a compound with known toxicity, it is likely to share those toxic properties. These fingerprints or signatures are most useful and refined when they contain expression information from a large number of genes and gene families. Ideally, a genome-wide measurement of expression provides the highest quality signature. Even genes whose expression is not altered by any tested compounds are important as well, as the levels of expression of these genes are used to normalize the rest of the expression data. The normalization procedure is useful for comparison of expression data after treatment with different compounds. While the assignment of gene function to elements of a toxicant signature aids in interpretation of toxicity mechanisms, knowledge of gene function is not necessary for the statistical matching of signatures which leads to prediction of toxicity. (See, for example, Press Release 00-02 from the National Institute of Environmental Health Sciences, released Feb. 29, 2000, available at http://www.niehs.nih.gov/oc/news/toxchip.htm.) Therefore, it is important and desirable in toxicological screening using toxicant signatures to include all expressed gene sequences.

[0308] In one embodiment, the toxicity of a test compound is assessed by treating a biological sample containing nucleic acids with the test compound. Nucleic acids that are expressed in the treated biological sample are hybridized with one or more probes specific to the polynucleotides of the present invention, so that transcript levels corresponding to the polynucleotides of the present invention may be quantified. The transcript levels in the treated biological sample are compared with levels in an untreated biological sample. Differences in the transcript levels between the two samples are indicative of a toxic response caused by the test compound in the treated sample.

[0309] Another particular embodiment relates to the use of the polypeptide sequences of the present invention to analyze the proteome of a tissue or cell type. The term proteome refers to the global pattern of protein expression in a particular tissue or cell type. Each protein component of a proteome can be subjected individually to further analysis. Proteome expression patterns, or profiles, are analyzed by quantifying the number of expressed proteins and their relative abundance under given conditions and at a given time. A profile of a cell's proteome may thus be generated by separating and analyzing the polypeptides of a particular tissue or cell type. In one embodiment, the separation is achieved using two-dimensional gel electrophoresis, in which proteins from a sample are separated by isoelectric focusing in the first dimension, and then according to molecular weight by sodium dodecyl sulfate slab gel electrophoresis in the second dimension (Steiner and Anderson, supra). The proteins are visualized in the gel as discrete and uniquely positioned spots, typically by staining the gel with an agent such as Coomassie Blue or silver or fluorescent stains. The optical density of each protein spot is generally proportional to the level of the protein in the sample. The optical densities of equivalently positioned protein spots from different samples, for example, from biological samples either treated or untreated with a test compound or therapeutic agent, are compared to identify any changes in protein spot density related to the treatment. The proteins in the spots are partially sequenced using, for example, standard methods employing chemical or enzymatic cleavage followed by mass spectrometry. The identity of the protein in a spot may be determined by comparing its partial sequence, preferably of at least 5 contiguous amino acid residues, to the polypeptide sequences of the present invention. In some cases, further sequence data may be obtained for definitive protein identificationl

[0310] A proteomic profile may also be generated using antibodies specific for REMAP to quantify the levels of REMAP expression. In one embodiment, the antibodies are used as elements on a microarray, and protein expression levels are quantified by exposing the microarray to the sample and detecting the levels of protein bound to each array element (Lueking, A. et al. (1999) Anal. Biochem. 270:103-111; Mendoze, L. G. et al. (1999) Biotechniques 27:778-788). Detection maybe performed by a variety of methods known in the art, for example, by reacting the proteins in the sample with a thiol- or amino-reactive fluorescent compound and detecting the amount of fluorescence bound at each array element.

[0311] Toxicant signatures at the proteome level are also useful for toxicological screening, and should be analyzed in parallel with toxicant signatures at the transcript level. There is a poor correlation between transcript and protein abundances for some proteins in some tissues (Anderson, N. L. and J. Seilhamer (1997) Electrophoresis 18:533-537), so proteome toxicant signatures may be useful in the analysis of compounds which do not significantly affect the transcript image, but which alter the proteomic profile. In addition, the analysis of transcripts in body fluids is difficult, due to rapid degradation of mRNA, so proteomic profiling may be more reliable and informative in such cases.

[0312] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins that are expressed in the treated biological sample are separated so that the amount of each protein can be quantified. The amount of each protein is compared to the amount of the corresponding protein in an untreated biological sample. A difference in the amount of protein between the two samples is indicative of a toxic response to the test compound in the treated sample. Individual proteins are identified by sequencing the amino acid residues of the individual proteins and comparing these partial sequences to the polypeptides of the present invention.

[0313] In another embodiment, the toxicity of a test compound is assessed by treating a biological sample containing proteins with the test compound. Proteins from the biological sample are incubated with antibodies specific to the polypeptides of the present invention. The amount of protein recognized by the antibodies is quantified. The amount of protein in the treated biological sample is compared with the amount in an untreated biological sample. A difference in the amount of protein between the two samples is indicative of a toxic response to the test compound in the treated sample.

[0314] Microarrays may be prepared, used, and analyzed using methods known in the art (See, e.g., Brennan, T. M. et al. (1995) U.S. Pat. No. 5,474,796; Schena, M. et al. (1996) Proc. Natl. Acad. Sci. USA 93:10614-10619; Baldeschweiler et al. (1995) PCT application WO95/251116; Shalon, D. et al. (1995) PCT application WO95/35505; Heller, R. A. et al. (1997) Proc. Natl. Acad. Sci. USA 94:2150-2155; and Heller, M. J. et al. (1997) U.S. Pat. No. 5,605,662.) Various types of microarrays are well known and thoroughly described in DNA Microarrays: A Practical Approach, M. Schena, ed. (1999) Oxford University Press, London, hereby expressly incorporated by reference.

[0315] In another embodiment of the invention, nucleic acid sequences encoding REMAP maybe used to generate hybridization probes useful in mapping the naturally occurring genomic sequence. Either coding or noncoding sequences may be used, and in some instances, noncoding sequences may be preferable over coding sequences. For example, conservation of a coding sequence among members of a multi-gene family may potentially cause undesired cross hybridization during chromosomal mapping. The sequences may be mapped to a particular chromosome, to a specific region of a chromosome, or to artificial chromosome constructions, e.g., human artificial chromosomes (HACs), yeast artificial chromosomes (YACs), bacterial artificial chromosomes (BACs), bacterial P1 constructions, or single chromosome cDNA libraries. (See, e.g., Harrington, J. J. et al. (1997) Nat. Genet 15:345-355; Price, C. M. (1993) Blood Rev. 7:127-134; and Trask, B. J. (1991) Trends Genet. 7:149-154.) Once mapped, the nucleic acid sequences of the invention may be used to develop genetic linkage maps, for example, which correlate the inheritance of a disease state with the inheritance of a particular chromosome region or restriction fragment length polymorphism (RFLP). (See, for example, Lander, E. S. and D. Botstein (1986) Proc. Natl. Acad. Sci. USA 83:7353-7357.)

[0316] Fluorescent in situ hybridization (FISH) may be correlated with other physical and genetic map data. (See, e.g., Heinz-Ulich, et al. (1995) in Meyers, supra, pp. 965-968.) Examples of genetic map data can be found in various scientific journals or at the Online Mendelian Inheritance in Man (OMIM) World Wide Web site. Correlation between the location of the gene encoding REMAP on a physical map and a specific disorder, or a predisposition to a specific disorder, may help define the region of DNA associated with that disorder and thus may further positional cloning efforts.

[0317] In situ hybridization of chromosomal preparations and physical mapping techniques, such as linkage analysis using established chromosomal markers, maybe used for extending genetic maps. Often the placement of a gene on the chromosome of another mammalian species, such as mouse, may reveal associated markers even if the exact chromosomal locus is not known. This information is valuable to investigators searching for disease genes using positional cloning or other gene discovery techniques. Once the gene or genes responsible for a disease or syndrome have been crudely localized by genetic linkage to a particular genomic region, e.g., ataxia-telangiectasia to 11q22-23, any sequences mapping to that area may represent associated or regulatory genes for further investigation. (See, e.g., Gatti, R. A. et al. (1988) Nature 336:577-580.) The nucleotide sequence of the instant invention may also be used to detect differences in the chromosomal location due to translocation, inversion, etc., among normal, carrier, or affected individuals.

[0318] In another embodiment of the invention, REMAP, its catalytic or immunogenic fragments, or oligopeptides thereof can be used for screening libraries of compounds in any of a variety of drug screening techniques. The fragment employed in such screening may be free in solution, affixed to a solid support, borne on a cell surface, or located intracellularly. The formation of binding complexes between REMAP and the agent being tested may be measured.

[0319] Another technique for drug screening provides for high throughput screening of compounds having suitable binding affinity to the protein of interest. (See, e.g., Geysen, et al. (1984) PCT application WO84/03564.) In this method, large numbers of different small test compounds are synthesized on a solid substrate. The test compounds are reacted with REMAP, or fragments thereof, and washed. Bound REMAP is then detected by methods well known in the art. Purified REMAP can also be coated directly onto plates for use in the aforementioned drug screening techniques. Alternatively, non-neutralizing antibodies can be used to capture the peptide and immobilize it on a solid support.

[0320] In another embodiment, one may use competitive drug screening assays in which neutralizing antibodies capable of binding REMAP specifically compete with a test compound for binding REMAP. In this manner, antibodies can be used to detect the presence of any peptide which shares one or more antigenic determinants with REMAP.

[0321] In additional embodiments, the nucleotide sequences which encode REMAP may be used in any molecular biology techniques that have yet to be developed, provided the new techniques rely on properties of nucleotide sequences that are currently known, including, but not limited to, such properties as the triplet genetic code and specific base pair interactions.

[0322] Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The following embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.

[0323] The disclosures of all patents, applications and publications, mentioned above and below, including U.S. Ser. No. 60/267,201, U.S. Ser. No. 60/269,580, U.S. Ser. No. 60/282,679, and U.S. Ser. No. 60/288,295, and U.S. Ser. No. [Attorney docket No. PF-1349 P filed Jan. 14, 2002], are expressly incorporated by reference herein.

EXAMPLES

[0324] I. Construction of cDNA Libraries

[0325] Incyte cDNAs were derived from cDNA libraries described in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.). Some tissues were homogenized and lysed in guanidinium isothiocyanate, while others were homogenized and lysed in phenol or in a suitable mixture of denaturants, such as TRIZOL (Life Technologies), a monophasic solution of phenol and guanidine isothiocyanate. The resulting lysates were centrifuged over CsCl cushions or extracted with chloroform. RNA was precipitated from the lysates with either isopropanol or sodium acetate and ethanol, or by other routine methods.

[0326] Phenol extraction and precipitation of RNA were repeated as necessary to increase RNA purity. In some cases, RNA was treated with DNase. For most libraries, poly(A)+ RNA was isolated using oligo d(T)-coupled paramagnetic particles (Promega), OLIGOTEX latex particles (QIAGEN, Chatsworth Calif.), or an OLIGOTEX mRNA purification kit (QIAGEN). Alternatively, RNA was isolated directly from tissue lysates using other RNA isolation kits, e.g., the POLY(A)PURE mRNA purification kit (Ambion, Austin Tex.).

[0327] In some cases, Stratagene was provided with RNA and constructed the corresponding cDNA libraries. Otherwise, cDNA was synthesized and cDNA libraries were constructed with the UNIZAP vector system (Stratagene) or SUPERSCRIPT plasmid system (Life Technologies), using the recommended procedures or similar methods known in the art. (See, e.g., Ausubel, 1997, supra, units 5.1-6.6.) Reverse transcription was initiated using oligo d(T) or random primers. Synthetic oligonucleotide adapters were ligated to double stranded cDNA, and the cDNA was digested with the appropriate restriction enzyme or enzymes. For most libraries, the cDNA was size-selected (300-1000 bp) using SEPHACRYL S1000, SEPHAROSE CL2B, or SEPHAROSE CL4B column chromatography (Amersham Pharmacia Biotech) or preparative agarose gel electrophoresis. cDNAs were ligated into compatible restriction enzyme sites of the polylinker of a suitable plasmid, e.g., PBLUESCRIPT plasmid (Stratagene), PSPORT1 plasmid (ife Technologies), PcDNA2.1 plasmid (Invitrogen, Carlsbad Calif.), PBK-CMV plasmid (Stratagene), PCR2-TOPOTA plasmid Invitrogen), PCMV-ICIS plasmid (Stratagene), pIGEN (hncyte Genomics, Palo Alto Calif.), pRARE (Incyte Genomics), or pINCY (Incyte Genomics), or derivatives thereof. Recombinant plasmids were transformed into competent E. coli cells including XL1-Blue, XL1-BlueMRF, or SOLR from Stratagene or DH5a, DH10B, or ElectroMAX DH10B from Life Technologies.

[0328] II. Isolation of cDNA Clones

[0329] Plasmids obtained as described in Example I were recovered from host cells by in vivo excision using the UNIZAP vector system (Stratagene) or by cell lysis. Plasmids were purified using at least one of the following: a Magic or WIZARD Minipreps DNA purification system (Promega); an AGTC Miniprep purification kit (edge Biosystems, Gaithersburg Md.); and QIAWELL 8 Plasmid, QIAWELL 8 Plus Plasmid, QIAWELL 8 Ultra Plasmid purification systems or the R.E.A.L. PREP 96 plasmid purification kit from QIAGEN. Following precipitation, plasmids were resuspended in 0.1 ml of distilled water and stored, with or without lyopbilization, at 4° C.

[0330] Alternatively, plasmid DNA was amplified from host cell lysates using direct link PCR in a high-throughput format (Rao, V. B. (1994) Anal. Biochem. 216:1-14). Host cell lysis and thermal cycling steps were carried out in a single reaction mixture. Samples were processed and stored in 384-well plates, and the concentration of amplified plasmid DNA was quantified fluorometrically using PICOGREEN dye (Molecular Probes, Eugene Oreg.) and a FLUOROSKAN II fluorescence scanner (Labsystems Oy, Helsinki, Finland).

[0331] II. Sequencing and Analysis

[0332] Incyte cDNA recovered in plasmids as descnbed in Example II were sequenced as follows. Sequencing reactions were processed using standard methods or high-throughput instrumentation such as the ABI CATALYST 800 (Applied Biosystems) thermal cycler or the PTC-200 thermal cycler (MJ Research) in conjunction with the HYDRA microdispenser (Robbins Scientific) or the MICROLAB 2200 (Hamilton) liquid transfer system. cDNA sequencing reactions were prepared using reagents provided by Amersham Pharmacia Biotech or supplied in ABI sequencing kits such as the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems). Electrophoretic separation of cDNA sequencing reactions and detection of labeled polynucleotides were carried out using the MBGABACE 1000 DNA sequencing system (Molecular Dynamics); the ABI PRISM 373 or 377 sequencing system (Applied Biosystems) in conjunction with standard ABI protocols and base calling software; or other sequence analysis systems known in the art. Reading frames within the cDNA sequences were identified using standard methods (reviewed in Ausubel, 1997, supra, unit 7.7). Some of the cDNA sequences were selected for extension using the techniques disclosed in Example VIII.

[0333] The polynucleotide sequences derived from Incyte cDNAs were validated by removing vector, linker, and poly(A) sequences and by masking ambiguous bases, using algorithms and programs based on BLAST, dynamic programming, and dinucleotide nearest neighbor analysis. The Incyte cDNA sequences or translations thereof were then queried against a selection of public databases such as the GenBank primate, rodent, mammalian, vertebrate, and eukaryote databases, and BLOCKS, PRINTS, DOMO, PRODOM; PROTEOME databases with sequences from Homo sapiens, Rattus norveaicus, Mus musculus, Caenorhabditis elegans, Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Candida albicans (Incyte Genomics, Palo Alto Calif.); hidden Markov model (HBW-based protein family databases such as PFAM; and HMM-based protein domain databases such as SMART (Schultz et al. (1998) Proc. Natl. Acad. Sci. USA 95:5857-5864; Letunic, I. et al. (2002) Nucleic Acids Res. 30:242-244). (HIM is a probabilistic approach which analyzes consensus primary structures of gene families. See, for example, Eddy, S. R. (1996) Curr. Opin. Struct. Biol. 6:361-365.) The queries were performed using programs based on BLAST, FASTA, BLIMPS, and HMMER. The Incyte cDNA sequences were assembled to produce full length polynucleotide sequences. Alternatively, GenBank cDNAs, GenBank ESTs, stitched sequences, stretched sequences, or Genscan-predicted coding sequences (see Examples IV and V) were used to extend Incyte cDNA assemblages to full length. Assembly was performed using programs based on Phred, Phrap, and Consed, and cDNA assemblages were screened for open reading frames using programs based on GeneMark, BLAST, and FASTA. The full length polynucleotide sequences were translated to derive the corresponding full length polypeptide sequences. Alternatively, a polypeptide of the invention may begin at any of the methionine residues of the full length translated polypeptide. Full length polypeptide sequences were subsequently analyzed by querying against databases such as the GenBank protein databases (genpept), SwissProt, the PROTEOME databases, BLOCKS, PRINTS, DOMO, PRODOM, Prosite, hidden Markov model (HMM-based protein family databases such as PPAM; and HMM-based protein domain databases such as SMART. Full length polynucleotide sequences are also analyzed using MACDNASIS PRO software (Hitachi Software Engineering, South San Francisco Calif.) and LASERGENE software (DNASTAR). Polynucleotide and polypeptide sequence alignments are generated using default parameters specified by the CLUSTAL algorithm as incorporated into the MEGALIGN multisequence alignment program (DNASTAR), which also calculates the percent identity between aligned sequences.

[0334] Table 7 summarizes the tools, programs, and algorithms used for the analysis and assembly of Incyte cDNA and full length sequences and provides applicable descriptions, references, and threshold parameters. The first column of Table 7 shows the tools, programs, and algorithms used, the second column provides brief descriptions thereof, the third column presents appropriate references, all of which are incorporated by reference herein in their entirety, and the fourth column presents, where applicable, the scores, probability values, and other parameters used to evaluate the strength of a match between two sequences (the higher the score or the lower the probability value, the greater the identity between two sequences).

[0335] The programs described above for the assembly and analysis of full length polynucleotide and polypeptide sequences were also used to identify polynucleotide sequence fragments from SEQ ID NO:44-86. Fragments from about 20 to about 4000 nucleotides which are useful in hybridization and amplification technologies are described in Table 4, column 2.

[0336] IV. Identification and Editing of Coding Sequences from Genomic DNA

[0337] Putative receptors and membrane-associated proteins were initially identified by running the Genscan gene identification program against public genomic sequence databases (e.g., gbpri and gbhtg). Genscan is a general-purpose gene identification program which analyzes genomic DNA sequences from a variety of organisms (See Burge, C. and S. Karlin (1997) J. Mol. Biol. 268:78-94, and Burge, C. and S. Karlin (1998) Curr. Opin. Struct. Biol. 8:346-354). The program concatenates predicted exons to form an assembled cDNA sequence extending from a methionine to a stop codon. The output of Genscan is a FASTA database of polynucleotide and polypeptide sequences. The maximum range of sequence for Genscan to analyze at once was set to 30 kb. To determine which of these Genscan predicted cDNA sequences encode receptors and membrane-associated proteins, the encoded polypeptides were analyzed by querying against PFAM models for receptors and membrane-associated proteins. Potential receptors and membrane-associated proteins were also identified by homology to Incyte cDNA sequences that had been annotated as receptors and membrane-associated proteins. These selected Genscan-predicted sequences were then compared by BLAST analysis to the genpept and gbpri public databases. Where necessary, the Genscan-predicted sequences were then edited by comparison to the top BLAST hit from genpept to correct errors in the sequence predicted by Genscan, such as extra or omitted exons. BLAST analysis was also used to find any Incyte cDNA or public cDNA coverage of the Genscan-predicted sequences, thus providing evidence for transcription. When Incyte cDNA coverage was available, this information was used to correct or confirm the Genscan predicted sequence. Full length polynucleotide sequences were obtained by assembling Genscan-predicted coding sequences with Incyte cDNA sequences and/or public cDNA sequences using the assembly process described in Example III. Alternatively, full length polynucleotide sequences were derived entirely from edited or unedited Genscan-predicted coding sequences.

[0338] V. Assembly of Genornic Sequence Data with cDNA Sequence Data

[0339] “Stitched” Sequences

[0340] Partial cDNA sequences were extended with exons predicted by the Genscan gene identification program descnbed in Example IV. Partial cDNAs assembled as described in Example III were mapped to genomic DNA and parsed into clusters containing related cDNAs and Genscan exon predictions from one or more genomic sequences. Each cluster was analyzed using an algorithm based on graph theory and dynamic programming to integrate cDNA and genomic information, generating possible splice variants that were subsequently confirmed, edited, or extended to create a full length sequence. Sequence intervals in which the entire length of the interval was present on more than one sequence in the cluster were identified, and intervals thus identified were considered to be equivalent by transitivity. For example, if an interval was present on a cDNA and two genomic sequences, then all three intervals were considered to be equivalent This process allows unrelated but consecutive genomic sequences to be brought together, bridged by cDNA sequence. Intervals thus identified were then “stitched” together by the stitching algorithm in the order that they appear along their parent sequences to generate the longest possible sequence, as well as sequence variants. linkages between intervals which proceed along one type of parent sequence (cDNA to cDNA or genomic sequence to genomic sequence) were given preference over linkages which change parent type (cDNA to genomic sequence). The resultant stitched sequences were translated and compared by BLAST analysis to the genpept and gbpri public databases. Incorrect exons predicted by Genscan were corrected by comparison to the top BLAST hit from genpept. Sequences were further extended with additional cDNA sequences, or by inspection of genomic DNA, when necessary.

[0341] “Stretched” Sequences

[0342] Partial DNA sequences were extended to full length with an algorithm based on BLAST analysis. First, partial cDNAs assembled as described in Example III were queried against public databases such as the GenBank primate, rodent, mammalian, vertebrate, and eukaryote databases using the BLAST program. The nearest GenBank protein homolog was then compared by BLAST analysis to either Incyte cDNA sequences or GenScan exon predicted sequences described in Example IV. A chimeric protein was generated by using the resultant high-scoring segment pairs (HSPs) to map the translated sequences onto the GenBank protein homolog. Insertions or deletions may occur in the chimeric protein with respect to the original GenBank protein homolog. The GenBank protein homolog, the chimeric protein, or both were used as probes to search for homologous genomic sequences from the public human genome databases. Partial DNA sequences were therefore “stretched” or extended by the addition of homologous genomic sequences. The resultant stretched sequences were examined to determine whether it contained a complete gene.

[0343] VI. Chromosomal Mapping of REMAP Encoding Polynucleotides

[0344] The sequences which were used to assemble SEQ ID NO:44-86 were compared with sequences from the Incyte LWESEQ database and public domain databases using BLAST and other implementations of the Smith-Waterman algorithm. Sequences from these databases that matched SEQ ID NO:44-86 were assembled into clusters of contiguous and overlapping sequences using assembly algorithms such as Phrap (Table 7). Radiation hybrid and genetic mapping data available from public resources such as the Stanford Human Genome Center (SHGC), Whitehead Institute for Genome Research (WIGR), and Généthon were used to determine if any of the clustered sequences had been previously mapped. Inclusion of a mapped sequence in a cluster resulted in the assignment of all sequences of that cluster, including its particular SEQ ID NO:, to that map location.

[0345] Map locations are represented by ranges, or intervals, of human chromosomes. The map position of an interval, in centiMorgans, is measured relative to the terminus of the chromosome's p-arm. (The centiMorgan (cM) is a unit of measurement based on recombination frequencies between chromosomal markers. On average, 1 cM is roughly equivalent to 1 megabase (Mb) of DNA in humans, although this can vary widely due to hot and cold spots of recombination.) The cM distances are based on genetic markers mapped by Généthon which provide boundaries for radiation hybrid markers whose sequences were included in each of the clusters. Human genome maps and other resources available to the public, such as the NCBI “GeneMap'99” World Wide Web site (http://www.ncbi.nlm.nagov/genemap/), can be employed to determine if previously identified disease genes map within or in proximity to the intervals indicated above.

[0346] VII. Analysis of Polynucleotide Expression

[0347] Northern analysis is a laboratory technique used to detect the presence of a transcript of a gene and involves the hybridization of a labeled nucleotide sequence to a membrane on which RNAs from a particular cell type or tissue have been bound. (See, e.g., Sambrook, supra, ch. 7; Ausubel (1995) supra, ch. 4 and 16.)

[0348] Analogous computer techniques applying BLAST were used to search for identical or related molecules in cDNA databases such as GenBank or LIFESEQ (Incyte Genomics). This analysis is much faster than multiple membrane-based hybridizations. In addition, the sensitivity of the computer search can be modified to determine whether any particular match is categorized as exact or similar. The basis of the search is the product score, which is defined as: $\frac{{BLAST}\quad {Score} \times {Percent}\quad {{Identit}y}}{5 \times {mnimum}\quad \left\{ {{{length}\left( {{Seq}.\quad 1} \right)},{{length}\left( {{Seq}.\quad 2} \right)}} \right\}}$

[0349] The product score takes into account both the degree of similarity between two sequences and the length of the sequence match. The product score is a normalizd value between 0 and 100, and is calculated as follows: the BLAST score is multiplied by the percent nucleotide identity and the product is divided by (5 times the length of the shorter of the two sequences). The BLAST score is calculated by assigning a score of +5 for every base that matches in a high-scoring segment pair AHSP), and −4 for every mismatch. Two sequences may share more than one HSP (separated by gaps). If there is more than one HSP, then the pair with the highest BLAST score is used to calculate the product score. The product score represents a balance between fractional overlap and quality in a BLAST alignment. For example, a product score of 100 is produced only for 100% identity over the entire length of the shorter of the two sequences being compared. A product score of 70 is produced either by 100% identity and 70% overlap at one end, or by 88% identity and 100% overlap at the other. A product score of 50 is produced either by 100% identity and 50% overlap at one end, or 79% identity and 100% overlap.

[0350] Alternatively, polynucleotide sequences encoding REMAP are analyzed with respect to the tissue sources from which they were derived. For example, some fall length sequences are assembled, at least in part, with overlapping Incyte cDNA sequences (see Example III). Each cDNA sequence is derived from a cDNA library constructed from a human tissue. Each human tissue is classified into one of the following organ/tissue categories: cardiovascular system; connective tissue; digestive system; embryonic structures; endocrine system; exocrine glands; genitalia, female; genitalia, male; germ cells; hemic and immune system; liver; musculoskeletal system; nervous system; pancreas; respiratory system; sense organs; skin; stomatognathic system; unclassified/mixed; or urinary tract. The number of libraries in each category is counted and divided by the total number of libraries across all categories. Similarly, each human tissue is classified into one of the following disease/condition categories: cancer, cell line, developmental, inflammation, neurological, trauma, cardiovascular, pooled, and other, and the number of libraries in each category is counted and divided by the total number of libraries across all categories. The resulting percentages reflect the tissue- and disease-specific expression of cDNA encoding REMAP. cDNA sequences and cDNA library/tissue information are found in the LIFESEQ GOLD database (Incyte Genomics, Palo Alto Calif.).

[0351] In this manner, SEQ ID NO:44 was mapped to chromosome 3 within the interval from 30.4 to 43.0 centiMorgans. SEQ ID NO:68 was mapped to chromosome 3 within the interval from 60.0 to 65.1 centiMorgans.

[0352] VII. Extension of REMAP Encoding Polynucleotides

[0353] Full length polynucleotide sequences were also produced by extension of an appropriate fragment of the full length molecule using oligonucleotide primers designed from this fragment. One primer was synthesized to initiate 5′ extension of the known fragment, and the other primer was synthesized to initiate 3′extension of the known fragment. The initial primers were designed using OLIGO 4.06 software (National Biosciences), or another appropriate program, to be about 22 to 30 nucleotides in length, to have a GC content of about 50% or more, and to anneal to the target sequence at temperatures of about 68 ° C. to about 72° C. Any stretch of nucleotides which would result in hairpin structures and primer-primer dimerizations was avoided.

[0354] Selected human cDNA libraries were used to extend the sequence. If more than one extension was necessary or desired, additional or nested sets of primers were designed.

[0355] High fidelity amplification was obtained by PCR using methods well known in the art. PCR was performed in 96-well plates using the PTC-200 thermal cycler (MJ Research, Inc.). The reaction mix contained DNA template, 200 nmol of each primer, reaction buffer containing Mg²⁺, (NH₄)₂SO₄, and 2-mercaptoethanol, Taq DNA polymerase (Amersham Pharmacia Biotech), ELONGASE enzyme (Ife Technologies), and Pfu DNA polymerase (Stratagene), with the following parameters for primer pair PCI A and PCI B: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 60° C., 1 min; Step 4: 68° C., 2 min; Step 5: Steps 2, 3, and 4 repeated 20 times; Step 6: 68° C., 5 min; Step 7: storage at 4° C. In the alternative, the parameters for primer pair T7 and SK+ were as follows: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 57° C., 1 min; Step 4: 68° C., 2 min; Step 5: Steps 2, 3, and 4 repeated 20 times; Step 6: 68° C., 5 min; Step 7: storage at 4° C.

[0356] The concentration of DNA in each well was determined by dispensing 100 μl PICOGREEN quantitation reagent (0.25% (v/v) PICOGREEN; Molecular Probes, Eugene Oreg.) dissolved in 1× TE and 0.5 μl of undiluted PCR product into each well of an opaque fluorimeter plate (Corning Costar, Acton Mass.), allowing the DNA to bind to the reagent. The plate was scanned in a Fluoroskan II (Labsystems Oy, Helsinki, Finland) to measure the fluorescence of the sample and to quantify the concentration of DNA. A 5 μl to 10 ∞l aliquot of the reaction mixture was analyzed by electrophoresis on a 1% agarose gel to determine which reactions were successful in extending the sequence.

[0357] The extended nucleotides were desalted and concentrated, transferred to 384-well plates, digested with CviJI cholera virus endonuclease (Molecular Biology Research, Madison Wis.), and sonicated or sheared prior to religation into pUC 18 vector (Amersham Pharmacia Biotech). For shotgun sequencing, the digested nucleotides were separated on low concentration (0.6 to 0.8%) agarose gels, fragments were excised, and agar digested with Agar ACE (Promega). Extended clones were religated using T4 ligase (New England Biolabs, Beverly Mass.) into pUC 18 vector (Amersham Pharmacia Biotech), treated with Pfu DNA polymerase (Stratagene) to fill-in restriction site overhangs, and transfected into competent E. coli cells. Transformed cells were selected on antibiotic-containing media, and individual colonies were picked and cultured overnight at 37° C. in 384-well plates in LB/2× carb liquid media.

[0358] The cells were lysed, and DNA was amplified by PCR using Taq DNA polymerase (Amersham Pharmacia Biotech) and Pfu DNA polymerase (Stratagene) with the following parameters: Step 1: 94° C., 3 min; Step 2: 94° C., 15 sec; Step 3: 60° C., 1 min; Step 4: 72° C., 2 min; Step 5: steps 2, 3, and 4 repeated 29 times; Step 6: 72° C., 5 min; Step 7: storage at 4° C. DNA was quantified by PICOGREEN reagent (Molecular Probes) as described above. Samples with low DNA recoveries were reamplified using the same conditions as described above. Samples were diluted with 20% dimethysulfoxide (1:2, v/v), and sequenced using DYENAMIC energy transfer sequencing primers and the DYENAMIC DIRECT kit (Amersham Pharmacia Biotech) or the ABI PRISM BIGDYE Terminator cycle sequencing ready reaction kit (Applied Biosystems).

[0359] In like manner, full length polynucleotide sequences are verified using the above procedure or are used to obtain 5′ regulatory sequences using the above procedure along with oligonucleotides designed for such extension, and an appropriate genomnic library.

[0360] IX. Identification of Single Nucleotide Polymorphisms in REMAP Encoding Polynucleotides

[0361] Common DNA sequence variants known as single nucleotide polymorphisms (SNPs) were identified in SEQ ID NO:44-86 using the LIFESEQ database (Incyte Genomics). Sequences from the same gene were clustered together and assembled as described in Example III, allowing the identification of all sequence variants in the gene. An algorithm consisting of a series of filters was used to distinguish SNPs from other sequence variants. Preliminary filters removed the majority of basecall errors by requiring a minimum Phred quality score of 15, and removed sequence alignment errors and errors resulting from improper trimming of vector sequences, chimeras, and splice variants. An automated procedure of advanced chromosome analysis analysed the original chromatogram files in the vicinity of the putative SNP. Clone error filters used statistically generated algorithms to identify errors introduced during laboratory processing, such as those caused by reverse transcriptase, polymerase, or somatic mutation. Clustering error filters used statistically generated algorithms to identify errors resulting from clustering of close homologs or pseudogenes, or due to contamination by non-human sequences. A final set of filters removed duplicates and SNPs found in immunoglobulins or T-cell receptors.

[0362] Certain SNPs were selected for further characterization by mass spectrometry using the high throughput MASSARRAY system (Sequenom, Inc.) to analyze allele frequencies at the SNP sites in four different human populations. The Caucasian population comprised 92 individuals (46 male, 46 female), including 83 from Utah, four French, three Venezualan, and two Amish individuals. The African population comprised 194 individuals (97 male, 97 female), all African Americans. The Hispanic population comprised 324 individuals (162 male, 162 female), all Mexican Hispanic. The Asian population comprised 126 individuals (64 male, 62 female) with a reported parental breakdown of 43% Chinese, 31% Japanese, 13% Korean, 5% Vietnamese, and 8% other Asian. Allele frequencies were first analyzed in the Caucasian population; in some cases those SNPs which showed no allelic variance in this population were not further tested in the other three populations.

[0363] X. Labeling and Use of Individual Hybridization Probes

[0364] Hybridization probes derived from SEQ ID NO:44-86 are employed to screen cDNAs, genomic DNAS, or mRNAs. Although the labeling of oligonucleotides, consisting of about 20 base pairs, is specifically described, essentially the same procedure is used with larger nucleotide 10 fragments. Oligonucleotides are designed using state-of-the-art software such as OLIGO 4.06 software (National Biosciences) and labeled by combining 50 μmol of each oligomer, 250 μCi of [γ-³²P] adenosine triphosphate (Amersham Pharmacia Biotech), and T4 polynucleotide kinase (DuPont NEN, Boston Mass.). The labeled oligonucleotides are substantially purified using a SEPHADEX G-25 superfine size exclusion dextran bead column (Amersham Pharmacia Biotech). An aliquot containing 10⁷ counts per minute of the labeled probe is used in a typical membrane-based hybridization analysis of human genomic DNA digested with one of the following endonucleases: Ase I, Bgl II, Eco RI, Pst I, Xba I, or Pvu II, (DuPont NEN).

[0365] The DNA from each digest is fractionated on a 0.7% agarose gel and transferred to nylon membranes (Nytran Plus, Schleicher & Schuell, Durham N.H.). Hybridization is carried out for 16 hours at 40° C. To remove nonspecific signals, blots are sequentially washed at room temperature under conditions of up to, for example, 0.1× saline sodium citrate and 0.5% sodium dodecyl sulfate. Hybridization patterns are visualized using autoradiography or an alternative imaging means and compared.

[0366] XI. Microarrays

[0367] The linkage or synthesis of array elements upon a microarray can be achieved utilizing photolithography, piezoelectric printing (ink-jet printing, See, e.g., Baldeschweiler, supra.), mechanical microspotting technologies, and derivatives thereof. The substrate in each of the aforementioned technologies should be uniform and solid with a non-porous surface (Schena (1999), supra). Suggested substrates include silicon, silica, glass slides, glass chips, and silicon wafers. Alternatively, a procedure analogous to a dot or slot blot may also be used to arrange and link elements to the surface of a substrate using thermal, UV, chemical, or mechanical bonding procedures. A typical array may be produced using available methods and machines well known to those of ordinary skill in the art and may contain any appropriate number of elements. (See, e.g., Schena, M. et al (1995) Science 270:467-470; Shalon, D. et al. (1996) Genome Res. 6:639-645; Marshall, A. and J. Hodgson (1998) Nat. Biotechnol. 16:27-31.)

[0368] Full length cDNAs, Expressed Sequence Tags (ESTs), or fragments or oligomers thereof may comprise the elements of the microarray. Fragments or oligomers suitable for hybridization can be selected using software well known in the art such as LASERGENE software (DNASTAR). The array elements are hybridized with polynucleotides in a biological sample. The polynucleotides in the biological sample are conjugated to a fluorescent label or other molecular tag for ease of detection. After hybridization, nonhybridized nucleotides from the biological sample are removed, and a fluorescence scanner is used to detect hybridization at each array element. Alternatively, laser desorbtion and mass spectrometry may be used for detection of hybridization. The degree of complementarity and the relative abundance of each polynucleotide which hybridizes to an element on the microarray may be assessed. In one embodiment, microarray preparation and usage is described in detail below.

[0369] Tissue or Cell Sample Preparation

[0370] Total RNA is isolated from tissue samples using the guanidinium thiocyanate method and poly(A)⁺RNA is purified using the oligo-(dT) cellulose method. Each poly(A)⁺ RNA sample is reverse transcribed using MMLV reverse-transcriptase, 0.05 pg/μl oligo-(dT) primer (2′mer), 1× first strand buffer, 0.03 units/μl RNase inhibitor, 500 μM dATP, 500 μM dGTP, 500 μM dTTP, 40 μM dCTP, 40 μM dCTP-Cy3 (BDS) or dCTP-Cy5 (Amersham Pharmacia Biotech). The reverse transcription reaction is performed in a 25 ml volume containing 200 ng poly(A)⁺ RNA with GEMBRIGHT kits (Incyte). Specific control poly(A)⁺ RNAs are synthesized by in vitro transcription from non-coding yeast genomic DNA. After incubation at 37° C. for 2 hr. each reaction sample (one with Cy3 and another with Cy5 labeling) is treated with 2.5 ml of 0.5M sodium hydroxide and incubated for 20 minutes at 85° C. to the stop the reaction and degrade the RNA. Samples are purified using two successive CHROMA SPIN 30 gel filtration spin columns (CLONTECH Laboratories, Inc. (CLONTECH), Palo Alto Calif.) and after combining, both reaction samples are ethanol precipitated using 1 ml of glycogen (1 mg/ml), 60 ml sodium acetate, and 300 ml of 100% ethanol. The sample is then dried to completion using a SpeedVAC (Savant Instruments Inc., Holbrook N.Y.) and resuspended in 14 μl 5× SSC/0.2% SDS.

[0371] Microarray Preparation

[0372] Sequences of the present invention are used to generate array elements. Each array element is amplified from bacterial cells containing vectors with cloned cDNA inserts. PCR amplification uses primers complementary to the vector sequences flanking the cDNA insert. Array elements are amplified in thirty cycles of PCR from an initial quantity of 1-2 ng to a final quantity greater than 5 μg. Amplified array elements are then purified using SEPHACRYI400 (Amersham Pharmacia Biotech).

[0373] Purified array elements are immobilized on polymer-coated glass slides. Glass microscope slides (Corning) are cleaned by ultrasound in 0.1% SDS and acetone, with extensive distilled water washes between and after treatments. Glass slides are etched in 4% hydrofluoric acid (VWR Scientific Products Corporation (VWR), West Chester Pa.), washed extensively in distilled water, and coated with 0.05% aminopropyl silane (Sigma) in 95% ethanol. Coated slides are cured in a 110° C. oven.

[0374] Array elements are applied to the coated glass substrate using a procedure described in U.S. Pat. No. 5,807,522, incorporated herein by reference. 1 μl of the array element DNA, at an average concentration of 100 ng/μl, is loaded into the open capillary printing element by a high-speed robotic apparatus. The apparatus then deposits about 5 nl of array element sample per slide.

[0375] Micro arrays are UV-crosslinked using a STRATALINKER UV-crosslinker (Stratagene). Microarrays are washed at room temperature once in 0.2% SDS and three times in distilled water. Non-specific binding sites are blocked by incubation of microarrays in 0.2% casein in phosphate buffered saline (PBS) (Tropix, Inc., Bedford Mass.) for 30 minutes at 60° C. followed by washes in 0.2% SDS and distilled water as before.

[0376] Hybridization

[0377] Hybridization reactions contain 9 μl of sample mixture consisting of 0.2 μg each of Cy3 and Cy5 labeled cDNA synthesis products in 5× SSC, 0.2% SDS hybridization buffer. The sample mixture is heated to 65° C. for 5 minutes and is aliquoted onto the microarray surface and covered with an 1.8 cm² coverslip. The arrays are transferred to a waterproof chamber having a cavity just slightly larger than a microscope slide. The chamber is kept at 100% humidity internally by the addition of 140 μl of 5× SSC in a corner of the chamber. The chamber containing the arrays is incubated for about 6.5 hours at 60° C. The arrays are washed for 10 min at 45° C. in a first wash buffer (1× SSC, 0.1% SDS), three times for 10 minutes each at 45° C. in a second wash buffer (0.1× SSC), and dried.

[0378] Detection

[0379] Reporter-labeled hybridization complexes are detected with a microscope equipped with an Innova 70 mixed gas 10 W laser (Coherent, Inc., Santa Clara Calif.) capable of generating spectral lines at 488 mm for excitation of Cy3 and at 632 nm for excitation of Cy5. The excitation laser light is focused on the array using a 20× microscope objective Nikon, Inc., Melville N.Y.). The slide containing the array is placed on a computer-controlled X-Y stage on the microscope and raster-scanned past the objective. The 1.8 cm×1.8 cm array used in the present example is scanned with a resolution of 20 micrometers.

[0380] In two separate scans, a mixed gas multiline laser excites the two fluorophores sequentially. Emitted light is split, based on wavelength, into two photomultiplier tube detectors (PMT R1477, Hamamatsu Photonics Systems, Bridgewater N.J.) corresponding to the two fluorophores. Appropriate filters positioned between the array and the photomultiplier tubes are used to filter the signals. The emission maxima of the fluorophores used are 565 nm for Cy3 and 650 nm for Cy5. Each array is typically scanned twice, one scan per fluorophore using the appropriate filters at the laser source, although the apparatus is capable of recording the spectra from both fluorophores simultaneously.

[0381] The sensitivity of the scans is typically calibrated using the signal intensity generated by a cDNA control species added to the sample mixture at a known concentration. A specific location on the array contains a complementary DNA sequence, allowing the intensity of the signal at that location to be correlated with a weight ratio of hybridizing species of 1:100,000. When two samples from different sources (e.g., representing test and control cells), each labeled with a different fluorophore, are hybridized to a single array for the purpose of identifying genes that are differentially expressed, the calibration is done by labeling samples of the calibrating cDNA with the two fluorophores and adding identical amounts of each to the hybridization mixture.

[0382] The output of the photomultiplier tube is digitized using a 12-bit RTI-835H analog-to-digital (A/D) conversion board (Analog Devices, Inc., Norwood Mass.) installed in an IBM-compatible PC computer. The digitized data are displayed as an image where the signal intensity is mapped using a linear 20-color transformation to a pseudocolor scale ranging from blue (low signal) to red (high signal). The data is also analyzed quantitatively. Where two different fluorophores are excited and measured simultaneously, the data are first corrected for optical crosstalk (due to overlapping emission spectra) between the fluorophores using each fluorophore's emission spectrum.

[0383] A grid is superimposed over the fluorescence signal image such that the signal from each spot is centered in each element of the grid. The fluorescence signal within each element is then integrated to obtain a numerical value corresponding to the average intensity of the signal. The software used for signal analysis is the GEMTOOLS gene expression analysis program (Incyte).

[0384] XII. Complementary Polynucleotides

[0385] Sequences complementary to the REMAP-encoding sequences, or any parts thereof, are used to detect, decrease, or inhibit expression of naturally occurring REMAP. Although use of oligonucleotides comprising from about 15 to 30 base pairs is described, essentially the same procedure is used with smaller or with larger sequence fragments. Appropriate oligonucleotides are designed using OLIGO 4.06 software (National Biosciences) and the coding sequence of REMAP. To inhibit transcription, a complementary oligonucleotide is designed from the most unique 5′ sequence and used to prevent promoter binding to the coding sequence. To inhibit translation, a complementary oligonucleotide is designed to prevent ribosomal binding to the REMAP-encoding transcript

[0386] XIII. Expression of REMAP

[0387] Expression and purification of REMAP is achieved using bacterial or virus-based expression systems. For expression of REMAP in bacteria, cDNA is subcloned into an appropriate vector containing an antibiotic resistance gene and an inducible promoter that directs high levels of cDNA transcription. Examples of such promoters include, but are not limited to, the trp-lac (tac) hybrid promoter and the T5 or T7 bacteriophage promoter in conjunction with the lac operator regulatory element. Recombinant vectors are transformed into suitable bacterial hosts, e.g., BL21(DE3). Antibiotic resistant bacteria express REMAP upon induction with isopropyl beta-D-thiogalactopyranoside (IPTG). Expression of REMAP in eukaryotic cells is achieved by infecting insect or mammalian cell lines with recombinant Autographica californica nuclear polyhedrosis virus (AcMNPV), commonly known as baculovirus. The nonessential polyhedrin gene of baculovirus is replaced with cDNA encoding REMAP by either homologous recombination or bacterial-mediated transposition involving transfer plasmid intermediates. Viral infectivity is maintained and the strong polyhedrin promoter drives high levels of cDNA transcription. Recombinant baculovirus is used to infect Spodoptera frugiperda (Sf9) insect cells in most cases, or human hepatocytes, in some cases. Infection of the latter requires additional genetic modifications to baculovirus. (See Engelhard, E. K. et al (1994) Proc. Natl. Acad. Sci. USA 91:3224-3227; Sandig, V. et al (1996) Hum. Gene Ther. 7:1937-1945.)

[0388] In most expression systems, REMAP is synthesized as a fusion protein with, e.g., glutathione S-transferase (GST) or a peptide epitope tag, such as FLAG or 6-His, permitting rapid, single-step, affinity-based purification of recombinant fusion protein from crude cell lysates. GST, a 26-kilodalton enzyme from Schistosoma japonicum, enables the purification of fusion proteins on immobilized glutathione under conditions that maintain protein activity and antigenicity (Amersham Pharmacia Biotech). Following purification, the GST moiety can be proteolytically cleaved from REMAP at specifically engineered sites. FLAG, an 8-amino acid peptide, enables immunoaffinity purification using commercially available monoclonal and polyclonal anti-FLAG antibodies (Eastman Kodak). 6-His, a stretch of six consecutive histidine residues, enables purification on metal-chelate resins (QIAGEN). Methods for protein expression and purification are discussed in Ausubel (1995, supra, ch. 10 and 16). Purified REMAP obtained by these methods can be used directly in the assays shown in Examples XVII and XVIII, where applicable.

[0389] XIV. Functional Assays

[0390] REMAP function is assessed by expressing the sequences encoding REMAP at physiologically elevated levels in mammalian cell culture systems. cDNA is subcloned into a mammalian expression vector containing a strong promoter that drives high levels of cDNA expression. Vectors of choice include PCMV SPORT (Life Technologies) and PCR3.1 (Invitrogen, Carlsbad Calif.), both of which contain the cytomegalovirus promoter. 5-10 μg of recombinant vector are transiently transfected into a human cell line, for example, an endothelial or hematopoietic cell line, using either liposome formulations or electroporation. 1-2 μg of an additional plasmid containing sequences encoding a marker protein are co-transfected. Expression of a marker protein provides a means to distinguish transfected cells from nontransfected cells and is a reliable predictor of cDNA expression from the recombinant vector. Marker proteins of choice include, e.g., Green Fluorescent Protein (GFP; Clontech), CD64, or a CD64-GFP fusion protein. Flow cytometry (FCM), an automated, laser optics-based technique, is used to identify transfected cells expressing GFP or CD64-GFP and to evaluate the apoptotic state of the cells and other cellular properties. FCM detects and quantifies the uptake of fluorescent molecules that diagnose events preceding or coincident with cell death. These events include changes in nuclear DNA content as measured by staining of DNA with propidium iodide; changes in cell size and granularity as measured by forward light scatter and 90 degree side light scatter; down-regulation of DNA synthesis as measured by decrease in bromodeoxynridine uptake; alterations in expression of cell surface and intracellular proteins as measured by reactivity with specific antibodies; and alterations in plasma membrane composition as measured by the binding of fluorescein-conjugated Annexin V protein to the cell surface. Methods in flow cytometry are discussed in Ormerod, M. G. (1994) Flow Cytometry, Oxford, New York N.Y.

[0391] The influence of REMAP on gene expression can be assessed using highly purified populations of cells transfected with sequences encoding REMAP and either CD64 or CD64-GFP. CD64 and CD64-GPP are expressed on the surface of transfected cells and bind to conserved regions of human immunoglobulin G (IgG). Transfected cells are efficiently separated from nontransfected cells using magnetic beads coated with either human IgG or antibody against CD64 (DYNAL, Lake Success N.Y.). mRNA can be purified from the cells using methods well known by those of skill in the art. Expression of mRNA encoding REMAP and other genes of interest can be analyzed by northern analysis or microarray techniques.

[0392] XV. Production of REMAP Specific Antibodies

[0393] REMAP substantially purified using polyacrylamide gel electrophoresis (PAGE; see, e.g., Harrington, M. G. (1990) Methods Enzymol. 182:488-495), or other purification techniques, is used to immunize animals (e.g., rabbits, mice, etc.) and to produce antibodies using standard protocols.

[0394] Alternatively, the REMAP amino acid sequence is analyzed using LASERGENE software (DNASTAR) to determine regions of high immunogenicity, and a corresponding oligopeptide is synthesized and used to raise antibodies by means known to those of skill in the art. Methods for selection of appropriate epitopes, such as those near the C-terminus or in hydrophilic regions are well described in the art. (See, e.g., Ausubel, 1995, supra, ch. 11.)

[0395] Typically, oligopeptides of about 15 residues in length are synthesized using an ABI 431A peptide synthesizer (Applied Biosystems) using FMOC chemistry and coupled to KLH (Sigma-Aldrich, St. Louis Mo.) by reaction with N-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) to increase immunogenicity. (See, e.g., Ausubel, 1995, supra.) Rabbits are immunized with the oligopeptide-KLH complex in complete Freund's adjuvant. Resulting antisera are tested for antipeptide and anti-REMAP activity by, for example, binding the peptide or REMAP to a substrate, blocking with 1% BSA, reacting with rabbit antisera, washing, and reacting with radio-iodinated goat anti-rabbit IgG.

[0396] XVI. Purification of Naturally Occurring REMAP Using Specific Antibodies

[0397] Naturally occurring or recombinant REMAP is substantially purified by immunoaffinity chromatography using antibodies specific for REMAP. An immunoaffinity column is constructed by covalently coupling anti-REMAP antibody to an activated chromatographic resin, such as CNBr-activated SEPHAROSE (Amersham Pharmacia Biotech). After the coupling, the resin is blocked and washed according to the manufacturer's instructions.

[0398] Media containing REMAP are passed over the immunoaffinity column, and the column is washed under conditions that allow the preferential absorbance of REMAP (e.g., high ionic strength buffers in the presence of detergent). The column is eluted under conditions that disrupt antibody/REMAP binding (e.g., a buffer of pH 2 to pH 3, or a high concentration of a chaotrope, such as urea or thiocyanate ion), and REMAP is collected.

[0399] XVII. Identification of Molecules which Interact with REMAP

[0400] REMAP, or biologically active fragments thereof, are labeled with ¹²⁵I Bolton-Hunter reagent. (See, e.g., Bolton, A. E. and W. M. Hunter (1973) Biochem. J. 133:529-539.) Candidate molecules previously arrayed in the wells of a multi-well plate are incubated with the labeled REMAP, washed, and any wells with labeled REMAP complex are assayed. Data obtained using different concentrations of REMAP are used to calculate values for the number, affinity, and association of REMAP with the candidate molecules.

[0401] Alternatively, molecules interacting with REMAP are analyzed using the yeast two-hybrid system as described in Fields, S. and O. Song (1989) Nature 340:245-246, or using commercially available kits based on the two-hybrid system, such as the MATCHMAKER system (Clontech).

[0402] REMAP may also be used in the PATHCALLING process (CuraGen Corp., New Haven Conn.) which employs the yeast two-hybrid system in a high-throughput manner to determine all interactions between the proteins encoded by two large libraries of genes (Nandabalan, K_(a) et al. (2000) U.S. Pat. No. 6,057,101).

[0403] XVIII. Demonstration of REMAP Activity

[0404] Gap Junction Activity of REMAP

[0405] Gap junction activity of REMAP is demonstrated as the ability to induce the formation of intercellular channels between paired Xenopus laevis oocytes injected with REMAP cRNA (Hennemann, supra). One week prior to the experimental injection with REMAP cRNA, oocytes are injected with antisense oligonucleotide to REMAP to reduce background. REMAP cRNA-injected oocytes are incubated overnight, stripped of vitelline membranes, and paired for recording of junctional currents by dual cell voltage clamp. The measured conductances are proportional to gap junction activity of REMAP.

[0406] Alternatively, an assay for REMAP activity measures the ion channel activity of REMAP using an electrophysiological assay for ion conductance. REMAP can be expressed by transforming a mammalian cell line such as COS7, HeLa or CHO with a eukaryotic expression vector encoding REMAP. Eukaryotic expression vectors are commercially available, and the techniques to introduce them into cells are well known to those skilled in the art. A second plasmid which expresses any one of a number of marker genes, such as β-galactosidase, is co-transformed into the cells to allow rapid identification of those cells which have taken up and expressed the foreign DNA. The cells are incubated for 48-72 hours after transformation under conditions appropriate for the cell line to allow expression and accumulation of REMAP and β-galactosidase.

[0407] Transformed cells expressing β-galactosidase are stained ble when a suitable colorimetric substrate is added to the culture media under conditions that are well known in the art. Stained cells are tested for differences in membrane conductance by electrophysiological techniques that are well known in the art. Untransformed cells, and/or cells transformed with either vector sequences alone or β-galactosidase sequences alone, are used as controls and tested in parallel. Cells expressing REMAP will have higher anion or cation conductance relative to control cells. The contribution of REMAP to conductance can be confirmed by incubating the cells using antibodies specific for REMAP. The antibodies will bind to the extracellular side of REMAP, thereby blocking the pore in the ion channel, and the associated conductance.

[0408] Transmembrane Protein Activity of REMAP

[0409] An assay for REMAP activity measures the expression of REMAP on the cell surface. cDNA encoding REMAP is transfected into an appropriate mammalian cell line. Cell surface proteins are labeled with biotin as descnbed (de la Fuente, M. A. et al (1997) Blood 90:2398-2405). Itmunoprecipitations are performed using REMAP-specific antibodies, and immunoprecipitated samples are analyzed using SDS-PAGE and immunoblotting techniques. The ratio of labeled immunoprecipitant to unlabeled immunoprecipitant is proportional to the amount of REMAP expressed on the cell surface.

[0410] An alternative assay for REMAP activity is based on a prototypical assay for ligand/receptor-mediated modulation of cell proliferation. This assay measures the amount of newly synthesized DNA in Swiss mouse 3T3 cells expressing REMAP. An appropriate mammalian expression vector containing cDNA encoding REMAP is added to quiescent 3T3 cultured cells using transfection methods well known in the art. The transfected cells are incubated in the presence of [³H]thymidine and varying amounts of REMAP ligand. Incorporation of [³H]thymidine into acid-precipitable DNA is measured over an appropriate time interval using a tritium radioisotope counter, and the amount incorporated is directly proportional to the amount of newly synthesized DNA. A linear dose-response curve over at least a hundred-fold REMAP ligand concentration range is indicative of receptor activity. One unit of activity per milliliter is defined as the concentration of REMAP producing a 50% response level, where 100% represents maxial incorporation of [³H]thymidine into acid-precipitable. DNA (McKay, I. and Leigh, I., eds. (1993) Growth Factors: A Practical Approach, Oxford University Press, New York, N.Y., p. 73).

[0411] An assay for REMAP activity measures the expression of REMAP on the cell surface. cDNA encoding REMAP is transfected into an appropriate mammalian cell line. Cell surface proteins are labeled with biotin as descnbed (de la Fuente, M. A. et al. (1997) Blood 90:2398-2405). Immunoprecipitations are performed using REMAP-specific antibodies, and immunoprecipitated samples are analyzed using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and immunoblotting techniques. The ratio of labeled immunoprecipitant to unlabeled immunoprecipitant is proportional to the amount of REMAP expressed on the cell surface.

[0412] In the alternative, an assay for REMAP activity is based on a prototypical assay for ligand/receptor-mediated modulation of cell proliferation. This assay measures the rate of DNA synthesis in Swiss mouse 3T3 cells. A plasmid containing polynucleotides encoding REMAP is added to quiescent 3T3 cultured cells using transfection methods well known in the art. The transiently transfected cells are then incubated in the presence of [³H]thymidine, a radioactive DNA precursor molecule. Varying amounts of REMAP ligand are then added to the cultured cells. Incorporation of [³H]thymidine into acid-precipitable DNA is measured over an appropriate time interval using a radioisotope counter, and the amount incorporated is directly proportional to the amount of newly synthesized DNA. A linear dose-response curve over at least a hundred-fold REMAP ligand concentration range is indicative of receptor activity. One unit of activity per milliliter is defined as the concentration of REMAP producing a 50% response level, where 100% represents maximal incorporation of [³H]thymidine into acid-precipitable DNA (McKay, I. and I. Leigh, eds. (1993) Growth Factors: A Practical Approach, Oxford University Press, New York N.Y., p.73.)

[0413] In a further alternative, the assay for REMAP activity is based upon the ability of GPCR family proteins to modulate G protein-activated second messenger signal transduction pathways (e.g., cAMP; Gaudin, P. et al. (1998) J. Biol. Chem. 273:4990-4996). A plasmid encoding full length REMAP is transfected into a mammalian cell line (e.g., Chinese hamster ovary (CHO) or human embryonic kidney (HEK-293) cell lines) using methods well-known in the art. Transfected cells are grown in 12-well trays in culture medium for 48 hours, then the culture medium is discarded, and the attached cells are gently washed with PBS. The cells are then incubated in culture medium with or without ligand for 30 minutes, then the medium is removed and cells lysed by treatment with 1 M perchloric acid. The cAMP levels in the lysate are measured by radioimmunoassay using methods well-known in the art. Changes in the levels of cAMP in the lysate from cells exposed to ligand compared to those without ligand are proportional to the amount of REMAP present in the transfected cells.

[0414] To measure changes in inositol phosphate levels, the cells are grown in 24-well plates containing 1×10⁵ cells/well and incubated with inositol-free media and [³H]myoinositol, 2 mCi/well, for 48 hr. The culture medium is removed, and the cells washed with buffer containing 10 mM LiCl followed by addition of ligand. The reaction is stopped by addition of perchloric acid. Inositol phosphates are extracted and separated on Dowex AG1-X8 (Bio-Rad) anion exchange resin, and the total labeled inositol phosphates counted by liquid scintillation. Changes in the levels of labeled inositol phosphate from cells exposed to ligand compared to those without ligand are proportional to the amount of REMAP present in the transfected cells.

[0415] In a further alternative, the ion conductance capacity of REMAP is demonstrated using an electrophysiological assay. REMAP is expressed by transforming a mammalian cell line such as COS7, HeLa or CHO with a eukaryotic expression vector encoding REMAP. Eukaryotic expression vectors are commercially available, and the techniques to introduce them into cells are well known to those skilled in the art. A small amount of a second plasmid, which expresses any one of a number of marker genes such as b-galactosidase, is co-transformed into the cells in order to allow rapid identification of those cells which have taken up and expressed the foreign DNA. The cells are incubated for 48-72 hours after transformation under conditions appropriate for the cell line to allow expression and accumulation of REMAP and b-galactosidase. Transformed cells expressing b-galactosidase are stained blue when a suitable calorimetric substrate is added to the culture media under conditions that are well known in the art. Stained cells are tested for differences in membrane conductance due to various ions by electrophysiological techniques that are well known in the art. Untransformed cells, and/or cells transformed with either vector sequences alone or b-galactosidase sequences alone, are used as controls and tested in parallel. The contribution of REMAP to cation or anion conductance can be shown by incubating the cells using antibodies specific for either REMAP. The respective antibodies will bind to the extracellular side of REMAP, thereby blocking the pore in the ion channel, and the associated conductance.

[0416] In a further alternative, REMAP transport activity is assayed by measuring uptake of labeled substrates into Xenopus laevis oocytes. Oocytes at stages V and VI are injected with REMAP mRNA (10 ng per oocyte) and incubated for 3 days at 18° C. in OR2 medium (82.5 mM NaCl, 2.5 mM KCl, 1 mM CaCl₂, 1 mM MgCl₂, 1 mM Na₂HPO₄, 5 mM Hepes, 3.8 mM NaOH, 50 μg/ml gentamycin, pH 7.8) to allow expression of REMAP protein. Oocytes are then transferred to standard uptake medium (100 mM NaCl, 2 mM KCl, 1 mM CaCl₂, 1 mM MgCl, 10 mM Hepes/Tris pH 7.5). Uptake of various substrates (e.g., amino acids, sugars, drugs, and neurotransmitters) is initiated by adding a ³H substrate to the oocytes. After incubating for 30 minutes, uptake is terminated by washing the oocytes three times in Na⁺-free medium, measuring the incorporated ³H, and comparing with controls. REMAP activity is proportional to the level of internalized ³H substrate.

[0417] In a further alternative, REMAP protein kinase (PK) activity is measured by phosphorylation of a protein substrate using gamma-labeled [³²P]-ATP and quantitation of the incorporated radioactivity using a gamma radioisotope counter. REMAP is incubated with the protein substrate, [³²P]-ATP, and an appropriate kinase buffer. The ³²P incorporated into the product is separated from free [³²P]-ATP by electrophoresis and the incorporated ³²P is counted. The amount of ³²P recovered is proportional to the PK activity of REMAP in the assay. A determination of the specific amino acid residue phosphorylated is made by phosphoamino acid analysis of the hydrolyzed protein.

[0418] Further, adenylyl cylcase activity of REMAP is demonstrated by the ability to convert ATP to cAMP (Mittal, C. K. (1986) Methods Enzymol. 132:422-428). In this assay REMAP is incubated with the substrate [α-³²P]ATP, following which the excess substrate is separated from the product cyclic [³²P]AMP. REMAP activity is determined in 12×75 mm disposable culture tubes containing 5 μl of 0.6 M Tris-HCl, pH 7.5, 5 μl of 0.2 M MgCl₂, 5 μl of 150 mM creatine phosphate containing 3 units of creatine phosphokinase, 5 μl of 4.0 mM 1-methyl-3-isobutyxanthine, 5 μl of 20 mM cAMP, 5 μl 20 mM dithiothreitol, 5 μl of 10 mM ATP, 10 μl [α-³²P]ATP (2-4×10⁶ cpm), and water in a total volume of 100 μl. The reaction mixture is prewarmed to 30° C. The reaction is initiated by adding REMAP to the prewarmed reaction mixture. After 10-15 minutes of incubation at 30° C., the reaction is terminated by adding 25 μl of 30% ice-cold trichloroacetic acid (TCA). Zero-time incubations and reactions incubated in the absence of REMAP are used as negative controls. Products are separated by ion exchange chromatography, and cyclic [³²P] AMP is quantified using a β-radioisotope counter. The REMAP activity is proportional to the amount of cyclic [³²P] AMP formed in the reaction.

[0419] Various modifications and variations of the described methods and systems of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with certain embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the descried modes for carrying out the invention which are obvious to those skilled in molecular biology or related fields are intended to be within the scope of the following claims. TABLE 1 Incyte Poly- Incyte Project Polypeptide Incyte nucleotide Polynucleotide ID SEQ ID NO: Polypeptide ID SEQ ID NO: ID 2489747 1 2489747CD1 44 2489747CB1 5857405 2 5857405CD1 45 5857405CB1 2891329 3 2891329CD1 46 2891329CB1 7474130 4 7474130CD1 47 7474130CB1 2109928 5 2109928CD1 48 2109928CB1 2675716 6 2675716CD1 49 2675716CB1 1953366 7 1953366CD1 50 1953366CB1 3992330 8 3992330CD1 51 3992330CB1 4043652 9 4043652CD1 52 4043652CB1 5540353 10 5540353CD1 53 5540353CB1 5632328 11 5632328CD1 54 5632328CB1 6727209 12 6727209CD1 55 6727209CB1 6923150 13 6923150CD1 56 6923150CB1 2589084 14 2589084CD1 57 2589084CB1 7950559 15 7950559CD1 58 7950559CB1 6981966 16 6981966CD1 59 6981966CB1 1287125 17 1287125CD1 60 1287125CB1 2924950 18 2924950CD1 61 2924950CB1 3471345 19 3471345CD1 62 3471345CB1 3615852 20 3615852CD1 63 3615852CB1 4973984 21 4973984CD1 64 4973984CB1 2122511 22 2122511CD1 65 2122511CB1 55009131 23 55009131CD1  66 55009131CB1  1538253 24 1538253CD1 67 1538253CB1 030658 25  030658CD1 68  030658CB1 7486348 26 7486348CD1 69 7486348CB1 3359663 27 3359663CD1 70 3359663CB1 3237418 28 3237418CD1 71 3237418CB1 2529616 29 2529616CD1 72 2529616CB1

[0420] TABLE 1 Incyte Poly- Incyte Project Polypeptide Incyte nucleotide Polynucleotide ID SEQ ID NO: Polypeptide ID SEQ ID NO: ID 7475662 30 7475662CD1 73 7475662CB1 3811024 31 3811024CD1 74 3811024CB1 1683407 32 1683407CD1 75 1683407CB1 1319969 33 1319969CD1 76 1319969CB1 1645034 34 1645034CD1 77 1645034CB1 7949783 35 7949783CD1 78 7949783CB1 1265361 36 1265361CD1 79 1265361CB1 2645814 37 2645814CD1 80 2645814CB1 695481 38  695481CD1 81  695481CB1 699941 39  699941CD1 82  699941CB1 1515839 40 1515839CD1 83 1515839CB1 2300766 41 2300766CD1 84 2300766CB1 7505816 42 7505816CD1 85 7505816CB1 7504118 43 7504118CD1 86 7504118CB1

[0421] TABLE 2 Polypeptide GenBank ID NO: SEQ Incyte or PROTEOME Probability ID NO: Polypeptide ID ID NO: Score Annotation 1 2489747CD1 g6650678 0.00E+00 [Mus musculus] nuclear pore membrane glycoprotein POM210 2 5857405CD1 g7259265 1.40E−31 [Mus musculus] contains transmembrane (TM) region. Inoue, S. et al. (2000) Biochem. Biophys. Res. Commun. 268: 553-561. 3 2891329CD1 g9837305 9.50E−111 [Rattus norvegicus] secretory carrier membrane protein 4 4 7474130CD1 g15077418 1.00E−153 gastric cancer multidrug resistance-associated protein [Homo sapiens] 4 7474130CD1 g662994 2.70E−55 [Homo sapiens] GPI-anchored protein p137. Ellis, J. A. (1995) J. Biol. Chem. 270: 20717-20723. 5 2109928CD1 g4514653 1.20E−223 [Homo sapiens] vascular Rab-GAP/TBC-containing protein. Yonekura, H. et al. (1999) Nucleic Acids Res. 27: 2591-2600. 18 2924950CD1 g14336748 1.00E−177 similar to protein kinase C substrate [Homo sapiens] 21 4973984CD1 g4193489 6.80E−192 [Rattus norvegicus] GLUT4 vesicle protein. Morris, N. J. et al. (1999) Biochim. Biophys. Acta 1431: 525-530. 22 2122511CD1 g10444345 5.10E−128 [Homo sapiens] CIG30 (membrane glycoprotein) 25  30658CD1 g7542723 1.40E−167 [Homo sapiens] DHHC1 protein 26 7486348CD1 g11527086 4.50E−97 [Mus musculus] folate receptor 3. Spiegelstein, O. et al. (2000) Gene 258: 117-125. 27 3359663CD1 g3372648 4.20E−55 [Homo sapiens] vesicle associated membrane protein-1B. Isenmann, S. et al. (1988) Mol. Biol. Cell 9: 1649-1660. 30 7475662CD1 g2815901 9.10E−284 [Homo sapiens] delayed-rectifier K+ channel alpha subunit. Shepard, A. R. and Rae, J. L. (1999) Am. J. Physiol. 277: c412-C424. 31 3811024CD1 g6707799 3.10E−23 [Homo sapiens] NK inhibitory receptor 37 2645814CD1 g4079809 3.30E−25 HERC2 [Homo sapiens]. Walkowicz, M. et al. (1999) Mamm. Genome 10: 870-878. Ji, Y. et al. (1999) Hum. Mol. Genet. 8: 533-542. 37 2645814CD1 g15823640 0 Als2 [Mus musculus] 43 7504118CD1 g309074 8.40E−38 [Mus musculus] 19.5 protein. MacLeod, C. et al. (1990) Cell Growth and Differ. 1: 271-279.

[0422] TABLE 3 Amino Potential SEQ Incyte Acid Gly- Potential ID Polypeptide Resi- Phosphorylation cosylation Analytical Methods NO: ID dues Sites Sites Signature Sequences, Domains and Motifs and Databases 1 2489747CD1 1887 S58, S77, S133, N44, N337, Signal cleavage: M1-A25 SPSCAN S165, S194, S215, N405, N484, S326, S377, S427, N681, N801, S577, S623, S632, N926, S658, S699, S781, N1039, S811, S829, S870, N1116, S898, S928, S1230, N1135, S1319, S1349, N1362, S1568, S1659, N1441 S1874, T59, T124, T181, T362, T419, T475, T498, T505, T572, T683, T994, T1061, T1089, T1149, T1215, T1310, T1427, T1499, T1545, T1595, T1651, T1705, T1833, T1844, Y227, Y922 Signal Peptide: M1-A24, M1-A25 HMMER Bacterial Ig-like domain (group 2): A1071-V1152 HMMER-PFAM Transmembrane domains: A3-I30, P951-Q979, TMAP T1043-N1069, F1112-G1140, L1482-E1502, Q1801-H1829; N-terminus is cytosolic INTEGRAL MEMBRANE GLYCOPROTEIN BLAST-PRODOM PRECURSOR GP210 TRANSMEMBRANE NUCLEAR PROTEIN SIGNAL SIMILARITY: PD044313: L10-L769, PD044312: L883-I1645, PD149488: S1798-H1887 2 5857405CD1 240 T37, T100, S109, N35, N175 Signal Peptide: M1-Q21 HMMER Y125, Y134, S211, T221, T224 Immunoglobulin domain: G41-V129 HMMER-PFAM Transmembrane domains: L6-R34; N-terminus is non- TMAP cytosolic 3 2891329CD1 266 S18, S39, S249, N61, N244 Transmembrane domains: R79-W99, S104-V124, TMAP T231 S139-W166, F177-A205; N-terminus is non-cytosolic PROTEIN SECRETORY MEMBRANE CARRIER- BLAST-PRODOM ASSOCIATED TRANSMEMBRANE TRANSPORT MULTIGENE FAMILY F11P17.4 F21B7.17: PD010192: L110-G230, PD013656: K41-G109 4 7474130CD1 824 S3, S16, S189, N9, N145, Signal cleavage: M1-A36 SPSCAN S208, S257, S264, N185, N443, S268, S274, S300, N587, N675, S338, S345, S473, N761 S485, S556, S590, S724, S738, S778, T39, T180, T216, T295, T327, T365, T371, T395, T412, T430, T444, T463, T750, Y299 Paraneoplastic encephalomyelitis antigen family BLIMPS-PRINTS signature: PR00961: T135-H150, T261-M276 GPI-ANCHORED PROTEIN P137 GPI-ANCHOR: BLAST-PRODOM PD043788: K51-I484 5 2109928CD1 1026 S31, S36, S48, S95, N173, N771 TBC domain: V268-C480 HMMER-PFAM S129, S164, S174, S175, S197, S227, S275, S323, S593, S701, S708, S746, S899, S912, S932, S1002, S1015, S1017, T94, T111, T159, T195, T261, T498, T532, T539, T559, T563, T564, T579, T645, T684, T916, T963 Transmembrane domains: S430-Y456 D627-F655; N- TMAP terminus is cytosolic Probable rabGAP domain: PF00566: I316-P325, BLIMPS-PFAM Y355-N360 PROTEIN CHROMOSOME TRANSMEMBRANE BLAST-PRODOM CELL DIVISION I OF ONCOGENE COSMID SIMILAR: PD001799: I316-L478 6 2675716CD1 70 N3 Signal cleavage: M1-S38 SPSCAN Signal Peptide: M1-S20, M1-W24 HMMER Transmembrane domains: F9-G37; N-terminus is non- TMAP cytosolic Neuromodulin (GAP-43) signatures PROFILESCAN (neuromodulin_2.prf): T35-K65 Serine proteases subtilase family active sites PROFILESCAN (subtilase_his.prf): S34-S70 7 1953366CD1 168 S44, S155, T50, N110 Signal cleavage: M1-L26 SPSCAN T94, T129, T151, Y81 Transmembrane domains: K8-E36; N-terminus is non- TMAP cytosolic 8 3992330CD1 71 N37, N59 Signal cleavage: M1-F18 SPSCAN Signal Peptide: M1-S20 HMMER Transmembrane domains: M1-I26, S38-N59; N- TMAP terminus is non-cytosolic 9 4043652CD1 126 Signal cleavage: M1-A19 SPSCAN Signal Peptide: M1-A19 HMMER Transmembrane domains: S4-H23; N-terminus is non- TMAP cytosolic 10 5540353CD1 91 S34, S82 Signal cleavage: M1-G61 SPSCAN Signal Peptide: M3-S36 HMMER Transmembrane domains: E41-L69; N-terminus is TMAP cytosolic 11 5632328CD1 73 T68, Y67 Signal cleavage: M1-R39 SPSCAN Signal Peptide: M1-Q25 HMMER Transmembrane domains: L15-R41; N-terminus is TMAP non-cytosolic ATP synthase alpha and beta subunits signature PROFILESCAN (atpase_alpha_beta.prf): V21-D64 12 6727209CD1 96 T61 Signal cleavage: M1-A26 SPSCAN Signal Peptide: M1-A26 HMMER Transmembrane domains: R31-R59; N-terminus is TMAP non-cytosolic 13 6923150CD1 89 T3, S20 Signal cleavage: M1-F48 SPSCAN Signal Peptide: M1-S20 HMMER Transmembrane domains: L17-K45; N-terminus is TMAP non-cytosolic TNFR/NGFR family cysteine-rich region proteins: BLIMPS-BLOCKS BL00652: L36-F42, C67-L77 14 2589084CD1 112 S5, T56, T68, S81, N53 Signal Peptide: M33-Q57 HMMER S93 15 7950559CD1 73 T40 Signal cleavage: M1-S34 SPSCAN Signal Peptide: M14-S34 HMMER Transmembrane domains: S10-K38 TMAP 16 6981966CD1 102 S45, S54 Signal cleavage: M1-T26 SPSCAN Transmembrane domains: E4-Q23; N-terminus is TMAP cytosolic 17 1287125CD1 96 N24 Signal cleavage: M1-G65 SPSCAN Transmembrane domains: L66-L85; N-terminus is TMAP cytosolic 18 2924950CD1 305 S68, S73, S136, N88, N115 Signal cleavage: M1-G17 SPSCAN S145, S277, T78, T90, T95, T179, T211, T221, T228, T286, Y218 Signal Peptide: M1-A24, M1-A22, M1-A20, M1-G17 HMMER Transmembrane domains: G4-A20; N-terminus is non- TMAP cytosolic Cell attachment sequence: R296-D298 MOTIFS 19 3471345CD1 144 S48, S74 Signal cleavage: M1-A52 SPSCAN Signal Peptide: M31-A52, M31-I55, M31-G62 HMMER Transmembrane domains: A19-F47, H91-R118; N- TMAP terminus is non-cytosolic 20 3615852CD1 434 S30, S34, S64, N32, N217 Transmembrane domains: R157-R185 TMAP S219, S232, S292, S301, S325, S327, S336, S386, T141, T170, T423, Y228 Vinculin signature: PR00806: C356-P366 BLIMPS-PRINTS 21 4973984CD1 845 S359, S437, S468, N123,, C2 domain (protein kinase C domain): L727-L816, HMMER-PFAM S474, S479, S556, N254,, L311-M397, L462-K541 S600, S609, S635, N435,, S672, S722, S760, N511,, S768, S785, T116, N567,, T125, T162, T223, N702 T414, T549, T569, T717, T765 Transmembrane domains: L40-A68, T223-K248; N- TMAP terminus is non-cytosolic C2 domain signature and profile (c2_domain.prf): PROFILESCAN I714-S768 C2 domain signature: PR00360: S741-L753, K770-S783 BLIMPS-PRINTS PROTEIN INTERGENIC REGION BLAST-PRODOM TRANSMEMBRANE REPEAT CLB1 CALB T12A2.15 CHROMOSOME XV: PD009833: R172- G309, D106-N268 C2-DOMAIN DM00150|P41823|149-276: L711-T839 BLAST-DOMO 22 2122511CD1 270 T112, T186, T231 N6, N110 Signal cleavage: M1-G51 SPSCAN GNS1/SUR4 family (transmembrane proteins): M1-S269 HMMER-PFAM Transmembrane domains: M26-Y54, F61-G81, G90- TMAP N110, K114-R139, L198-R224, H230-T257; N- terminus is non-cytosolic GNS1/SUR4 family proteins: BL01188: Y155-L205, BLIMPS-BLOCKS L242-Y258, K59-G90, K124-V154 PROTEIN TRANSMEMERANE GNS1 BLAST-PRODOM MEMBRANE GLYCOPROTEIN CHROMOSOME SIMILAR S CERVISIAE INTEGRAL: PD006965: F30-S269 DM02520|P49191|28-313: M55-R260, F29-R58 BLAST-DOMO 23 55009131CD1 2481 S1386, S1948, S54, N97, N689, TPR Domain (nuclear receptor): G514-V547, G474- HMMER-PFAM T266, S347, S606, N708, N870, L507, S314-S347, F714-V747, T1077-L1110, A834- S691, S868, S872, N1092, L867, C794-L827, C274-L307, A917-L950, A1117- S978, S1163, N1272, I1150, A754-L787, M434-L467, A674-L707, F58-N91, S1290, S1298, N1357 G1037-M1070, S997-T1030, C92-W125, G877-L910, S1316, T1318, A594-L627, A354-L387, P126-S159, A957-M990, S1339, S1441, G634-L667, A394-L427, A554-L587 S1506, T1538, T1578, S1590, S1594, 1607, S1625, T1840, S1936, S1953, T1980, S2006, T2069, S2139, T2141, S2149, T2253, S2258, S2279, S2335, S2387, S20, S96, S229, T250, S336, T1149, S1298, S1457, S1550, S1568, S1582, S1695, T1918, S2098, T2146, T2230, S2267, S2302, S2331, T2386, S2398, S2478, Y283, Y390, Y437, Y969, Y757 Transmembrane domains: G1234-I1257, T1642-I1669; TMAP N-terminus is cytosolic PROTEIN REPEAT TPR DOMAIN NUCLEAR, BLAST-PRODOM CONSERVED SIGNAL TRANSPORT RECEPTOR TRANSFERASE: PD000069: Q768-E1102, E451-H777 TPR REPEAT: DM00408|P31948|1-147: E57-P195 BLAST-DOMO 24 1538253CD1 78 N58 Signal cleavage: M1-A63 SPSCAN Signal Peptide: M41-A63, M41-S64 HMMER Transmembrane domains: L33-S59; N-terminus is non TMAP cytosolic 25 030658CD1 299 S134, T247 N109 DHHC zinc finger domain: L118-I182 HMMER-PFAM Transmembrane domains: R40-F60, Y73-S93, Q169- TMAP C197, W202-F230; N-terminus is cytosolic YOR034C; MEMBRANE: DM05142|Q09701|316-569: BLAST-DOMO I78-L195 Eukaryotic thiol (cysteine) proteases histidine active MOTIFS site: S183-H193 26 7486348CD1 243 S38, S186, S196, N73 Signal cleavage: M1-A19 SPSCAN T60, T141, T174 Signal Peptide: M1-A19 HMMER PROTEIN FOLATE RECEPTOR GLYCOPROTEIN BLAST-PRODOM PRECURSOR SIGNAL FOLATE-BINDING MEMBRANE GPI-ANCHOR MULTIGENE: PD006906: E22-S225 FOLATE-BINDING, PROTEIN BLAST-DOMO DM02165|P15328|22-256: W18-L242 27 3359663CD1 117 S30 S63 S77 N27 Synaptobrevin: P24-I112 HMMER-PFAM Synaptobrevin proteins BL00417: R33-Q60, K61-S114 BLIMPS_BLOCKS Synaptobrevin signature: T29-K85 PROFILESCAN Synaptobrevin signature PR00219: BLIMPS_PRINTS Q38-E57, R58-S77, M97-Y116 PROTEIN TRANSMEMBRANE BLAST_PRODOM SYNAPTOBREVIN SYNAPSE SYNAPTOSOME SIGNAL ANCHOR MEMBRANE VESICLE MULTIGENE FAMILY PD001229: N27-I112 SYNAPTOBREVIN DM00708|P23763|13-117: E13-V113 BLAST_DOMO SYNAPTOBREVIN DM00708|P47194|20-124: P17-V113 BLAST_DOMO SYNAPTOBREVIN DM00708|P35589|1-105: P17-V113 BLAST_DOMO SYNAPTOBREVIN DM00708|P18489|27-131: N27-V113 BLAST_DOMO Synaptobrevin signature: N51-D70 MOTIFS 28 3237418CD1 275 S22 S37 S270 S272 N233 Transmembrane domain: A8-N36, E46-Q65, N86-V112, TMAP T33 Y264 V112-Y134, R139-V159, I166-T186, C220-R246 N-terminus is non-cytosolic 19.5 Q60774_Mouse PD124939: M1-K257 BLAST_PRODOM 29 2529616CD1 268 S3 S60 S108 S222 N147 Transmembrane domain: I205-I221 TMAP T77 T81 T104 N-terminus is non-cytosolic T170 30 7475662CD1 848 S50 S63 S121 S177 N61 N262 Signal_Cleavage: M1-Q18 SPSCAN S232 S264 S272 S386 S497 S563 S610 S618 S694 S809 T55 T242 T331 T484 T690 T821 T825 Signal Peptide: M1-K26 HMMER K+ channel tetramerisation domain: E372-Y478 HMMER_PFAM Ion transport protein: C546-I778 HMMER_PFAM Transmembrane segments: Q4-K27 S541-A569 F623- TMAP G649 G657-L675 K692-A716 P751-F779 N-terminus cytosolic Potassium channel signature PR00169: E423-T442, BLIMPS_PRINTS P535-S563, R596-T619, F622-L642, L668-S694, E697-E720, F727-V749, G756-F782 Filaggrin signature PR00487: G257-G277, R400-D415 BLIMPS_PRINTS CHANNEL IONIC PROTEIN POTASSIUM BLAST_PRODOM SUBUNIT PD000141: F622-V796 PD060706: M323-S370 PD033026: S799-Y848 CHANNEL; POTASSIUM; CDRK; SHAW; BLAST_DOMO DM00490 JH0595|26-142: I365-Y478 P15387|18-134: I365-Y478 P17970|268-384: V376-Y478 DM00436|P15387|136-299: Q510-I671 31 3811024CD1 273 S26 S80 S84 S179 N96 Immunoglobulin domain: G30-V109 HMMER_PFAM S190 S202 T38 T74 T98 T137 T143 T189 T250 Transmembrane segments: D115-P133 P210-L238 N- TMAP terminus non-cytosolic IMMUNOGLOBULIN DM00001 BLAST_DOMO Q08708|44-120: Y39-E110 32 1683407CD1 311 S229 S297 T292 Transmembrane segments: Q13-V41 S92-V115 T165- TMAP T293 Y272 L191 P197-S219 N-terminus cytosolic 33 1319969CD1 169 T97 Signal_Cleavage: M1-A29 SPSCAN Transmembrane segments: T4-Y27 S43-L69 TMAP N-terminus non-cytosolic 34 1645034CD1 271 S38 S43 S62 S76 PAP2 superfamily: I118-T263 HMMER_PFAM S93 S108 S177 Transmembrane segments: V113-S137 L139-K167 TMAP V200-S228 V237-L256 N-terminus non-cytosolic PROTEIN TRANSMEMBRANE PHOSPHATIDIC BLAST_PRODOM ACID PHOSPHATASE HYDROLASE MEMBRANE TRANSPORT PERMEASE INTEGRAL PD002093: T119-V254 35 7949783CD1 388 S2 S30 S44 S353 N43 N380 Transmembrane segments: H65-A86 L140-S160 TMAP T10 T39 T87 T111 M169-A189 I198-K218 G227-T247 G268-I296 F319- T141 T254 T347 T347 N-terminus non-cytosolic 36 1265361CD1 726 S53 S108 S120 N140 N508 NHL repeat: L474-V502, F531-M559, F278-I304, HMMER_PFAM S337 S346 5373 N520 N658 L223-V251 S393 S440 S525 S600 T19 T30 T106 T235 T322 T435 T530 Transmembrane segments: C77-L96 C673-Y688 TMAP PROTEIN YKUV CY274.05 TRANSMEMBRANE BLAST_PRODOM YBDE PD016168: V54-L187 DM01687|P34611|567-612: E528-V558 BLAST_DOMO 37 2645814CD1 1651 S3 S7 S8 S138 N652 MORN (Membrane Occupation and Recognition HMMER_PFAM S266 S332 S338 Nexus) repeat: Y1100-V1122, Y1049-M1071, Y1072- S353 S356 S417 M1094, Y1221-Y1244, Y1198-I1220, F1151-R1171, S449 S465 S466 F1123-L1143 S479 S483 S492 S523 S638 S694 S781 S873 S906 S919 S1033 S1055 S1140 S1215 S1232 S1267 S1271 S1328 S1460 S1540 S1554 S1569 S1589 S1597 T9 T241 T243 T262 T313 T428 T575 T644 T701 T856 T977 T978 T989 T1170 T1219 T1327 T1448 T1455 T1546 T1567 T1578 T1643 Y891 Y1017 Y1049 Y1072 Y1084 Y1371 PH domain: N972-D1005 HMMER_PFAM Regulator of chromosome condensation: Q179-Q218, HMMER_PFAM E527-A576, Q579-G592, D59-G66, V150-I167, V43-E58 TRANSMEMBRANE SEGMENTS: H197-Q218 TMAP A391-V407 S781-L809 L925-Q947 F1594-I1614 N-terminus non-cytosolic Regulator of chromosome condensation (RCC1) PROFILESCAN signatures rcc1_1.prf: L564-G611 Chromosome condensation regulatoR RCC1 signature BLIMPS_PRINTS PR00633: E527-D543, V561-L574, V580-F596 PROTEIN BLAST_PRODOM PHOSPHATIDYLINOSITOL4PHOSPHATE 5KINASE PUTATIVE T22C1.7 ISOLOG ATPIP5K1: PD149995: G1056-K1292 PROTEIN REPEAT GUANINENUCLEOTIDE BLAST_PRODOM RELEASING FACTOR REGULATOR RJS CELL CYCLE MITOSIS PD001424: L521-D595 Immunoglobulins and major histo-compatibility MOTIFS complex proteins signature Y875-H881 Regulator of chromosome condensation (RCC1) MOTIFS signature 2 L155-L165 V206-L216 38 695481CD1 1112 S106 S188 S261 N220 N309 TRANSMEMBRANE SEGMENTS: T13-R40 S82-V101 TMAP S454 S732 S737 N482 N702 I228-C244 E276-K304 Q455-N482 L573-V590 S892 S902 S911 N923 Q952-R977 N-terminus non-cytosolic S932 S992 S1060 S1087 T44 T74 T137 T177 T212 T347 T412 T563 T654 T687 T830 T869 T918 T930 Y257 PROTEIN R06F6.8B R06F6.8 CHROMOSOME II BLAST_PRODOM TRANSMEMBRANE PD044316: H421-R703, H166-G377, H166-K417, V793-G1068, P686-S911, L19-V65, L90-S139, G675-S693 Leucine zipper pattern L529-L550 MOTIFS 39 699941CD1 832 S25 S114 S222 N15 N177 Domain of unknown function HMMER_PFAM S253 S397 S424 N266 N368 DUF221: K348-P809 S535 S603 S768 N406 N462 S779 S791 S792 N511 S800 S801 S820 S824 T76 T227 T268 T337 T388 T456 T700 T746 T814 Y93 Y151 Y264 TRANSMEMBRANE SEGMENTS: L36-K64 Y151-S179 TMAP N202-S222 S424-A452 P473-F501 M515-W543 V570-R597 A623-Y651 N682-R702 M711-G731 N-terminus non-cytosolic PROTEIN CHROMOSOME HYP1 BLAST_PRODOM TRANSMEMBRANE XII I ORF SIMILARITY ARABIDOPSIS F24O1.3 PD005475: G326-C724 40 1515839CD1 807 S58 S94 S149 S177 TRANSMEMBRANE SEGMENTS: A362-A380 TMAP S253 S267 S308 L446-L467 L467-R485 Q554-D572 S363 S376 S491 N-terminus cytosolic S499 S504 S776 T64 T167 T202 T212 T427 T462 T530 T613 T663 T738 Y186 Leucine zipper pattern L61-L82 L701-L722 L708-L729 MOTIFS Cell attachment sequence R358-D360 MOTIFS 41 2300766CD1 511 S8 S26 S87 S169 N48 N91 TRANSMEMBRANE SEGMENTS: F291-F319 TMAP S192 S276 S495 N249 N335 L336-L356 G364-I384 Q392-M412 I440-F460 T467-I487 T222 N494 N-terminus cytosolic Leucine zipper pattern L461-L482 MOTIFS 42 7505816CD1 476 S8 S26 S87 S169 N48 N91 Cytosolic domains: R320-P330, Q386-I405, W456-S476 TMHMMER S192 S276 S460 N249 N459 Transmembrane domains: H297-F319, W331-G353, T222 I363-L385, M406-A428, L433-V455 Non-cytosolic domains: M1-D296, H354-F362, T429-T432 Leucine zipper pattern: L426-L447 MOTIFS 43 7504118CD1 206 S22 S37 S201 S203 N164 signal_cleavage: M1-S22 SPSCAN T33 Y195 Signal Peptide: M1-S22 HMMER Cytosolic domains: T33-R44, D100-E105, S166-E206 TMHMMER Transmembrane domains: P10-H32, L45-V67, I77-R99, L106-P128, L143-Y165 Non-cytosolic domains: M1-L9, H68-H76, P129-N142 19.5 PD124939: V58-K188, M1-H76 BLAST_PRODOM

[0423] TABLE 4 Polynucleotide SEQ ID NO:/ Incyte ID/ Sequence Length Sequence Fragments 44/ 1-190, 12-284, 12-810, 18-632, 137-705, 434-1112, 517-1141, 616-846, 639-1025, 645-1271, 725-1310, 916-1175, 2489747CB1/ 929-1488, 971-1473, 1022-1547, 1059-1337, 1059-1538, 1176-1208, 1176-1651, 1225-1469, 1225-1517, 6625 1225-1807, 1240-1799, 1413-2063, 1685-1929, 1685-2031, 1950-2212, 1950-2622, 2082-2866, 2092-2892, 2099-2901, 2135-2693, 2178-2785, 2216-2855, 2216-2858, 2224-3028, 2262-2860, 2289-3046, 2362-2579, 2404-2860, 2432-3207, 2449-3217, 2468-3028, 2493-3338, 2527-3039, 2533-3044, 2747-3481, 2814-3660, 2862-3487, 2864-3470, 2869-3654, 2871-3541, 2898-3695, 2907-3620, 2948-3620, 2948-3663, 2951-3665, 2968-3636, 2969-3817, 2972-3584, 2983-3491, 2996-3859, 3001-3251, 3019-3528, 3035-3554, 3050-3941, 3055-3920, 3058-3894, 3065-3754, 3077-3858, 3091-3748, 3092-3788, 3098-3713, 3103-3857, 3103-3929, 3104-3810, 3109-3791, 3112-3852, 3116-3914, 3118-3993, 3130-3894, 3145-3783, 3151-3809, 3154-3732, 3155-3910, 3160-3818, 3165-3942, 3171-3219, 3196-3789, 3198-3929, 3205-3911, 3209-4004, 3210-4031, 3211-4045, 3230-4059, 3233-3736, 3235-4030, 3235-4054, 3236-3849, 3236-4009, 3245-3950, 3247-3739, 3248-3839, 3254-3904, 3254-4056, 3268-3713, 3281-4065, 3287-4122, 3304-3810, 3322-4011, 3327-4005, 3342-4035, 3353-4008, 3354-3947, 3356-4118, 3358-4143, 3367-4194, 3368-3766, 3382-3897, 3387-3901, 3397-4270, 3411-4245, 3422-3759, 3448-3966, 3463-4289, 3482-4141, 3482-4304, 3488-4113, 3506-4338, 3519-4194, 3543-4316, 3605-4194, 3636-4131, 3637-4125, 3642-4543, 3658-4458, 3670-4090, 3750-4328, 3755-4591, 3788-4388, 3864-4359, 3875-4164, 3875-4313, 3894-4567, 3905-4555, 3912-4378, 3913-4462, 3923-4750, 3943-4576, 3950-4701, 3981-4475, 3983-4861, 3989-4842, 3993-4558, 3995-4653, 4018-4816, 4019-4809, 4024-4824, 4030-4904, 4051-4684, 4051-4830, 4101-4665, 4114-4913, 4136-5005, 4145-4876, 4149-4853, 4154-5049, 4156-4902, 4163-5042, 4212-5072, 4215-4834, 4228-4865, 4234-4864, 4240-4938, 4240-4997, 4258-4929, 4261-4915, 4283-4874, 4289-4841, 4289-5009, 4292-5070, 4293-4815, 4295-4891, 4300-5121, 4319-4970, 4323-4960, 4323-5125, 4324-4961, 4351-4940, 4358-5178, 4362-4991, 4364-5064, 4375-5026, 4378-5013, 4396-4867, 4406-4672, 4412-4939, 4413-5147, 4488-5130, 4507-5041, 4508-4977, 4515-5015, 4517-5396, 4520-4879, 4522-4782, 4543-5026, 4546-5040, 4546-5059, 4550-5195, 4555-5251, 4559-5095, 4568-5396, 4572-4961, 4573-5213, 4574-4776, 4574-5078, 4575-4814, 4576-4671, 4600-5445, 4619-4885, 4627-5312, 4660-5507, 4660-5522, 4701-5285, 4701-5290, 4712-5288, 4766-5335, 4774-5547, 4788-5401, 4843-5451, 4843-5589, 4861-5568, 4890-5442, 4907-5730, 4911-5270, 4940-5492, 4941-5787, 4956-5802, 4960-5563, 4970-5779, 4971-5597, 4986-5604, 4986-5679, 4995-5708, 5002-5261, 5003-5231, 5005-5760, 5006-5518, 5029-5256, 5032-5881, 5045-5318, 5046-5889, 5056-5656, 5057-5324, 5070-5336, 5091-5302, 5100-5646, 5107-5386, 5110-5428, 5118-5813, 5120-5448, 5126-5502, 5129-5859, 5143-5333, 5149-5878, 5165-5838, 5166-5959, 5169-5730, 5183-5791, 5184-5467, 5185-5363, 5185-5364, 5188-5258, 5188-5415, 5188-5549, 5218-5591, 5229-6013, 5231-5519, 5234-5460, 5235-5928, 5244-6001, 5244-6004, 5252-6013, 5255-5943, 5258-5949, 5260-5441, 5270-5467, 5272-6008, 5276-5954, 5300-5989, 5318-6118, 5330-6040, 5355-5960, 5365-6009, 5412-6033, 5422-6245, 5439-6132, 5465-6060, 5468-6109, 5485-6343, 5495-6174, 5503-6140, 5521-6180, 5521-6312, 5528-6341, 5541-5960, 5586-6024, 5597-6308, 5612-6109, 5613-6242, 5626-6250, 5642-6126, 5642-6230, 5642-6266, 5645-6193, 5646-6237, 5661-6097, 5662-6371, 5670-6156, 5716-6300, 5718-6273, 5728-5998, 5744-6309, 5745-6026, 5745-6070, 5760-6391, 5795-6533, 5797-6062, 5816-6151, 5832-6115, 5839-6066, 5844-6072, 5844-6109, 5846-6094, 5846-6286, 5848-6168, 5851-6443, 5855-6072, 5858-6354, 5858-6487, 5858-6496, 5878-6103, 5883-6160, 5883-6447, 5891-6446, 5893-6531, 5899-6496, 5902-6142, 5906-6365, 5907-6182, 5909-6379, 5911-6018, 5911-6147, 5916-6069, 5918-6358, 5921-6414, 5922-6163, 5922-6402, 5931-6368, 5937-6546, 5938-6201, 5942-6197, 5949-6253, 5949-6505, 5953-6466, 5956-6232, 5959-6480, 5966-6207, 5966-6403, 5969-6221, 5973-6221, 5973-6246, 6307-6625, 6335-6625 45/ 1-236, 1-369, 1-397, 1-479, 1-523, 5-586, 25-432, 25-618, 37-94, 37-144, 60-285, 60-433, 63-439, 76-315, 107-220, 5857405CB1/ 133-610, 173-337, 271-527, 283-543, 288-809, 297-761, 314-584, 314-881, 393-976, 405-933, 414-933, 2962 420-1063, 430-703, 443-680, 463-1040, 465-1001, 486-761, 492-906, 492-933, 497-1102, 502-1112, 516-995, 543-1012, 551-1095, 603-1268, 604-1242, 670-1368, 673-1128, 684-1042, 694-1351, 699-1382, 718-1337, 751-1278, 752-1148, 771-1240, 794-1342, 820-1006, 877-1243, 885-1475, 891-1010, 898-1569, 911-1514, 916-1467, 918-1228, 925-1106, 927-1517, 929-1505, 939-1406, 986-1660, 1009-1257, 1143-1562, 1199-1287, 1240-1714, 1242-1790, 1246-1317, 1269-1749, 1342-1581, 1393-1816, 1403-1820, 1425-1681, 1507-2027, 1510-1769, 1595-1810, 1604-2244, 1616-2105, 1645-2139, 1655-1915, 1655-2111, 1722-2214, 1741-2402, 1743-2217, 1917-2158, 1917-2172, 1940-2183, 2006-2274, 2075-2307, 2078-2389, 2143-2333, 2143-2387, 2143-2425, 2181-2424, 2237-2780, 2249-2831, 2308-2422, 2309-2834, 2312-2911, 2323-2952, 2396-2958, 2440-2932, 2449-2941, 2486-2962, 2495-2951, 2495-2962, 2526-2904, 2530-2813, 2555-2584, 2566-2951, 2590-2952, 2639-2765, 2668-2951, 2695-2946 46/ 1-540, 12-238, 29-244, 29-500, 33-221, 33-246, 33-630, 38-303, 40-285, 42-652, 45-273, 45-295, 45-311, 45-340, 2891329CB1/ 49-318, 49-324, 54-314, 54-321, 56-206, 56-445, 66-629, 124-462, 198-447, 230-791, 367-541, 370-974, 1638 394-597, 394-744, 394-814, 394-921, 460-746, 527-695, 569-1058, 591-793, 591-1073, 607-760, 609-1063, 658-912, 678-863, 714-890, 762-1024, 763-1036, 875-1100, 875-1429, 920-1559, 928-1181, 934-1200, 970-1516, 971-1218, 981-1227, 1017-1284, 1028-1326, 1076-1305, 1147-1412, 1254-1548, 1280-1490, 1280-1528, 1333-1533, 1368-1554, 1368-1603, 1375-1638, 1395-1598 47/ 1-282, 1-535, 1-557, 1-649, 1-655, 1-671, 1-683, 1-757, 7-560, 10-600, 16-842, 25-564, 43-644, 76-669, 111-157, 7474130CB1/ 111-241, 111-268, 111-301, 113-370, 242-938, 272-515, 316-524, 317-717, 318-717, 327-583, 327-594, 3322 337-594, 374-643, 378-916, 391-695, 441-1155, 447-578, 452-1142, 460-980, 472-717, 479-717, 538-1179, 606-873, 801-1064, 801-1067, 801-1083, 801-1208, 802-861, 819-1194, 826-972, 849-1409, 923-1296, 927-1623, 967-1212, 978-1347, 1022-1603, 1072-1739, 1076-1495, 1122-1918, 1147-1683, 1213-1926, 1292-2064, 1303-1955, 1309-1871, 1321-1922, 1333-2134, 1338-1982, 1351-2132, 1351-2134, 1360-2064, 1379-1670, 1379-1899, 1420-1688, 1488-1953, 1495-2114, 1510-1953, 1547-2144, 1592-2144, 1600-1757, 1625-2134, 1629-2131, 1634-2325, 1637-1952, 1641-2121, 1644-1933, 1644-1952, 1651-2567, 1674-2364, 1691-1953, 1698-1952, 1703-1804, 1801-1952, 1868-2526, 1915-1953, 1949-2130, 1949-2131, 1949-2156, 1949-2169, 1950-2100, 1950-2136, 1952-2267, 1955-2239, 1977-2223, 1985-2269, 1995-2144, 2003-2267, 2014-2269, 2025-2269, 2050-2719, 2081-2269, 2099-2130, 2099-2200, 2099-2213, 2099-2238, 2099-2267, 2099-2269, 2100-2124, 2114-2269, 2149-2423, 2157-2491, 2161-2356, 2202-2269, 2229-2269, 2243-2269, 2267-2301, 2267-2318, 2267-2353, 2267-2392, 2267-2402, 2267-2415, 2267-2416, 2267-2423, 2267-2437, 2267-2448, 2267-2462, 2267-2491, 2267-2531, 2337-2491, 2339-2491, 2346-2974, 2349-2489, 2359-2973, 2386-3103, 2389-2491, 2395-2491, 2405-2491, 2428-3140, 2443-2491, 2449-2491, 2462-2491, 2466-2491, 2467-3173, 2468-2491, 2471-2491, 2486-3251, 2491-2536, 2491-2679, 2491-2740, 2491-2821, 2493-2536, 2534-2599, 2534-2600, 2534-3020, 2534-3106, 2535-2583, 2535-2600, 2535-2625, 2535-2660, 2535-2665, 2535-2670, 2535-2703, 2535-2717, 2535-2735, 2535-2755, 2535-2787, 2535-2805, 2535-2875, 2535-2923, 2535-2974, 2535-2976, 2535-2982, 2535-3019, 2535-3032, 2535-3090, 2535-3093, 2535-3104, 2535-3125, 2535-3227, 2538-2677, 2548-2873, 2554-3199, 2559-2600, 2572-3149, 2576-3209, 2579-3213, 2582-2733, 2582-2760, 2598-2630, 2598-2648, 2598-2693, 2598-2772, 2598-2869, 2598-3075, 2600-2961, 2600-3026, 2602-2719, 2603-3322, 2609-2809, 2611-2875, 2635-2750, 2643-3222, 2643-3306, 2644-3066, 2646-3306, 2662-3203, 3027-3248, 3027-3301, 3063-3151 48/ 1-386, 1-579, 14-100, 379-944, 388-612, 398-978, 400-814, 400-820, 426-1039, 426-1055, 447-1161, 482-1051, 2109928CB1/ 656-1135, 710-1331, 755-1344, 790-1319, 832-1084, 1131-1707, 1173-1654, 1173-1679, 1173-1702, 5278 1218-1765, 1228-1877, 1262-1714, 1300-1921, 1306-1925, 1359-1929, 1375-1964, 1424-1978, 1468-2097, 1498-2059, 1530-2016, 1535-1791, 1576-2243, 1805-2420, 1807-2417, 1837-2451, 1843-2481, 1854-2445, 1864-2347, 1886-2407, 1906-2567, 1915-2556, 1934-2542, 1944-2529, 1974-2645, 1979-2570, 1982-2531, 1992-2242, 1993-2637, 2083-2527, 2129-2763, 2184-2722, 2190-2761, 2213-2781, 2232-2452, 2238-2762, 2241-2783, 2253-2854, 2299-2545, 2309-2747, 2356-2729, 2363-2738, 2373-2956, 2375-2961, 2420-2974, 2438-3068, 2447-3077, 2462-2957, 2472-3100, 2476-3073, 2480-3100, 2481-3100, 2504-3100, 2526-3100, 2530-2803, 2530-3100, 2533-3100, 2535-3100, 2536-3100, 2538-3100, 2550-3100, 2552-3100, 2553-3091, 2557-3097, 2561-2604, 2563-3077, 2565-3100, 2574-2968, 2574-3099, 2574-3100, 2578-3100, 2586-3100, 2600-3100, 2602-3100, 2606-3100, 2787-3034, 2787-3280, 2854-3127, 2871-3134, 2878-3151, 2932-3515, 2953-3147, 3126-3289, 3180-3435, 3280-3547, 3355-3632, 3393-3951, 3464-3952, 3506-3801, 3526-3762, 3526-4035, 3766-4046, 3802-4181, 3810-4083, 3816-4084, 3906-4147, 3916-4185, 3919-4396, 3963-4181, 3964-4189, 4064-4333, 4092-4355, 4100-4382, 4115-4386, 4134-4387, 4146-4472, 4173-4487, 4174-4389, 4182-4460, 4210-4753, 4219-4491, 4224-4495, 4261-4502, 4275-4502, 4305-4616, 4312-4599, 4331-4501, 4368-4591, 4368-4938, 4375-4645, 4375-4653, 4393-4641, 4403-4566, 4405-4688, 4413-4696, 4436-4697, 4452-4712, 4457-4782, 4459-4730, 4474-4677, 4486-4760, 4505-4736, 4505-4950, 4515-4741, 4524-4743, 4551-4792, 4553-4840, 4553-4890, 4557-4788, 4562-4736, 4573-4868, 4577-4907, 4578-4723, 4589-4880, 4589-5136, 4592-5254, 4597-4847, 4598-4871, 4606-4862, 4607-4848, 4612-5242, 4648-4912, 4690-4951, 4693-4993, 4695-5278, 4707-5064, 4720-4939, 4733-4981, 4742-5024, 4744-5253, 4798-5053, 4806-5259, 4824-5023, 4846-5119, 4851-5263, 4875-5115, 4893-5177, 4904-5093, 4904-5164, 4944-5221, 4956-5201, 4959-5242, 4959-5277, 4962-5249, 4967-5273, 5005-5278, 5012-5243, 5013-5253, 5034-5253, 5034-5278, 5055-5278, 5116-5278 49/ 1-623, 110-166, 264-427, 280-772, 281-725, 295-384, 297-654, 301-558, 303-652, 304-747, 372-623, 376-623, 2675716CB1/ 526-780, 533-955, 551-1037, 551-1194, 552-726, 563-843, 564-786, 564-953, 566-658, 566-953, 566-977, 567-997, 1282 567-1024, 567-1070, 583-821, 585-777, 585-792, 586-818, 586-989, 591-1253, 593-1282, 595-1154, 599-964, 602-750, 615-1148, 624-1073, 635-1166, 658-1272, 674-1094, 687-981, 694-964, 717-1282, 726-1237, 729-925, 736-1029, 795-1058, 823-1070, 827-1238, 929-1194 50/ 1-242, 1-483, 7-290, 21-250, 130-339, 130-344, 174-482, 186-679, 246-742, 247-502, 254-482, 254-705, 256-482, 1953366CB1/ 260-735, 271-811, 291-832, 297-720, 318-648, 414-890, 481-747, 618-1223, 621-911, 723-764, 770-1206, 1550 810-1214, 870-1214, 892-1206, 932-1207, 1001-1550 51/ 1-554, 1-1522, 108-481, 163-667, 252-685, 252-805, 252-829, 252-840, 252-842, 252-879, 252-909, 256-917, 3992330CB1/ 273-904, 302-904, 323-943, 354-998, 355-900, 365-911, 397-987, 404-914, 437-1006, 463-1080, 474-1048, 1543 476-1059, 481-1004, 524-947, 563-1030, 568-1081, 584-1094, 597-965, 601-1251, 605-1083, 605-1117, 610-1152, 626-1251, 640-1223, 643-1223, 670-1272, 710-1094, 920-1543, 931-1514, 935-1523, 942-1524, 975-1543, 1053-1543, 1068-1543, 1069-1543, 1388-1543 52/ 1-270, 46-552, 179-504, 179-723, 191-475, 293-544, 293-582, 507-640, 526-801, 526-1013, 569-822, 603-859, 4043652CB1/ 603-1099, 825-1056, 827-906, 1031-1274, 1031-1334, 1049-1304, 1070-1332, 1096-1345, 1107-1332, 1156-1437, 1531 1185-1476, 1208-1423, 1217-1375, 1273-1531, 1274-1494 53/ 1-581, 282-474, 282-483, 282-683, 282-887, 282-922, 347-581 5540353CB1/ 922 54/ 1-241, 1-260, 1-277, 1-448, 1-454, 1-502, 1-530, 1-535, 1-543, 1-574, 1-582, 1-583, 1-584, 1-611, 1-612, 1-614, 5632328CB1/ 1-635, 1-637, 1-640, 1-646, 1-656, 1-657, 1-667, 1-670, 1-676, 1-682, 1-706, 1-707, 2-643, 3-657, 3-689, 5-398, 1378 13-727, 15-712, 21-643, 29-753, 41-798, 58-641, 72-798, 92-634, 103-752, 114-850, 146-877, 176-881, 177-813, 182-896, 486-1207, 523-1238, 529-988, 579-1197, 593-1112, 613-1050, 618-1133, 629-1338, 683-1378, 700-1378, 728-1378, 735-1378, 738-1378, 759-1378, 761-1378, 765-1378, 813-1339, 814-1378, 820-1378, 824-1378, 860-1196, 1049-1378, 1083-1378 55/ 1-688, 1-896, 80-900, 84-733, 84-871, 85-365, 87-643 6727209CB1/ 900 56/ 1-495, 1-692, 10-606, 479-1152 6923150CB1/ 1152 57/ 1-637, 32-743, 117-507, 151-570, 151-650, 151-719, 151-821, 155-562, 161-874, 167-521, 167-693, 169-522, 2589084CB1/ 169-874, 173-337, 173-521, 299-772, 304-521, 340-690, 384-839, 406-927, 446-1045, 503-1123, 528-1075, 1423 565-1049, 567-1130, 659-1115, 659-1130, 662-1130, 705-1178, 758-918, 837-1422, 852-1423, 965-1159, 967-1130 58/ 1-580, 101-646, 220-457, 328-1057, 465-957 7950559CB1/ 1057 59/ 1-478, 1-688 6981966CB1/ 688 60/ 1-298, 1-362, 1-495, 1-546, 1-550, 1-555, 1-568, 1-577, 1-587, 1-699, 1-716, 1-849, 5-539, 5-619, 34-805, 134-734, 1287125CB1/ 134-890, 163-745, 218-453, 369-874, 540-1252, 542-1252, 585-1252, 646-1252, 681-1249, 684-730, 750-1000, 1252 769-1193 61/ 1-175, 1-197, 1-228, 1-240, 2-450, 10-244, 10-245, 10-290, 10-297, 10-463, 10-509, 11-239, 11-260, 11-270, 2924950CB1/ 11-275, 11-305, 11-355, 11-446, 11-457, 12-128, 12-221, 14-108, 15-134, 15-241, 16-128, 17-128, 19-331, 20-263, 1208 20-264, 20-278, 20-483, 21-220, 21-446, 22-253, 22-487, 23-276, 23-280, 23-307, 24-298, 26-261, 26-277, 27-318, 28-280, 28-503, 29-290, 29-423, 30-437, 31-251, 31-655, 32-295, 33-277, 33-290, 33-298, 33-627, 34-328, 35-334, 46-128, 46-345, 47-315, 47-352, 50-335, 51-128, 54-276, 54-333, 69-311, 69-312, 69-321, 69-356, 100-352, 107-379, 127-173, 127-211, 128-166, 130-241, 130-515, 131-196, 145-412, 181-434, 181-747, 195-252, 195-469, 195-523, 195-627, 218-252, 218-843, 220-514, 221-252, 235-488, 235-773, 239-503, 243-562, 243-826, 247-334, 247-368, 247-391, 247-403, 247-425, 247-432, 247-441, 247-486, 247-647, 248-477, 248-530, 249-431, 251-360, 256-584, 259-566, 278-562, 282-552, 282-568, 289-543, 290-515, 294-542, 296-546, 303-561, 303-577, 306-534, 307-542, 331-636, 333-559, 333-823, 334-432, 334-532, 334-588, 353-619, 359-650, 373-983, 382-845, 382-929, 388-637, 388-659, 388-668, 393-957, 396-649, 396-661, 396-666, 396-670, 396-678, 398-653, 408-664, 427-543, 427-723, 432-728, 437-731, 440-756, 444-873, 447-708, 451-653, 461-708, 470-627, 470-738, 470-807, 473-714, 474-627, 476-712, 480-543, 484-748, 491-754, 495-738, 502-741, 509-760, 516-809, 519-778, 523-809, 525-755, 533-824, 535-791, 542-627, 542-998, 548-801, 548-805, 553-846, 560-849, 561-739, 561-1170, 566-778, 566-781, 568-839, 571-726, 571-824, 578-788, 580-627, 587-846, 591-840, 593-767, 593-884, 598-1036, 599-855, 602-828, 602-1174, 605-1208, 609-875, 614-888, 620-1208, 624-671, 624-713, 624-717, 624-733, 624-749, 624-842, 624-848, 624-888, 624-985, 624-1085, 624-1094, 624-1133, 626-883, 632-876, 632-1132, 632-1156, 633-894, 633-897, 633-911, 633-916, 633-925, 641-922, 644-1043, 644-1163, 648-1208, 649-1170, 651-869, 651-1105, 652-1090, 666-913, 680-866, 680-916, 681-1193, 683-944, 683-948, 683-979, 684-1157, 686-873, 686-944, 686-945, 688-1193, 698-1185, 704-1185, 710-989, 710-1208, 712-956, 713-1207, 715-1193, 718-957, 718-1149, 726-1193, 727-1208, 731-1193, 732-1193, 733-1007, 739-1004, 739-1193, 741-1080, 754-1034, 756-1193, 757-1197, 759-840, 759-1202, 760-1006, 763-1043, 764-1004, 765-1032, 768-1201, 768-1208, 770-1151, 772-1193, 778-927, 778-966, 779-1007, 781-1193, 786-1068, 787-1038, 790-1193, 794-1123, 795-1193, 798-1020, 800-1145, 804-1193, 809-1017, 813-1142, 813-1193, 815-1101, 815-1201, 819-1200, 820-1193, 823-1208, 838-960, 838-1097, 838-1202, 839-1193, 843-1193, 844-1200, 850-1193, 854-1116, 862-1208, 874-1185, 875-1208, 878-1165, 887-1193, 890-1193, 891-1203, 902-1166, 909-1193, 923-1185, 945-1171, 953-1193, 953-1208, 974-1208, 977-1156, 1002-1193, 1002-1198 62/ 1-126, 1-206, 1-231, 1-283, 1-527, 1-682, 9-735, 11-528, 23-267, 40-469, 48-182, 49-270, 50-155, 50-314, 68-295, 3471345CB1/ 214-385, 263-523, 414-983, 446-1077, 469-528, 548-983, 649-838, 852-938 1077 63/ 1-642, 26-271, 26-680, 34-338, 34-596, 39-271, 39-642, 44-784, 135-385, 135-681, 300-892, 300-946, 397-1221, 3615852CB1/ 562-1222, 567-1222, 585-1229, 665-1219, 688-1314, 734-1220, 929-1317, 980-1511, 981-1317, 1212-1492, 2053 1341-1593, 1341-1862, 1454-1927, 1457-1836, 1459-1835, 1659-1915, 1684-1927, 1797-2053 64/ 1-449, 1-600, 287-836, 436-993, 448-597, 466-1011, 479-2733, 490-595, 490-701, 518-795, 529-704, 561-1354, 4973984CB1/ 567-647, 604-1062, 626-920, 651-1198, 658-1264, 676-1239, 709-1426, 734-919, 734-920, 738-1190, 3250 760-1304, 863-1132, 863-1351, 863-1488, 894-994, 921-1019, 921-1188, 959-1212, 960-1447, 1042-1445, 1045-1305, 1045-1536, 1056-1504, 1061-1662, 1065-1583, 1074-1536, 1117-1413, 1124-1582, 1154-1356, 1154-1429, 1156-1634, 1163-1536, 1189-1435, 1251-1497, 1254-1500, 1254-1700, 1308-1537, 1308-1689, 1365-1536, 1366-1536, 1372-1884, 1379-1706, 1408-1537, 1419-1986, 1431-1702, 1519-2187, 1521-1763, 1536-1611, 1536-1683, 1536-1746, 1536-1954, 1551-1676, 1553-1772, 1553-1951, 1589-1776, 1610-1903, 1611-1699, 1634-1829, 1665-1937, 1676-1924, 1678-1950, 1683-2228, 1697-2044, 1701-2155, 1705-1942, 1707-2000, 1746-2002, 1761-2230, 1788-1850, 1801-2074, 1806-2052, 1821-2087, 1902-1944, 1911-2618, 1936-2516, 1945-2185, 1946-2221, 1989-2247, 2037-2283, 2037-2531, 2037-2622, 2314-2624, 2323-2582, 2340-2808, 2408-2997, 2417-2985, 2434-2979, 2440-3222, 2448-2949, 2477-2742, 2481-2715, 2483-2939, 2517-2769, 2529-2766, 2533-2790, 2536-2795, 2553-2775, 2564-2807, 2576-2878, 2579-2965, 2581-2847, 2587-3231, 2604-3236, 2607-2859, 2611-2941, 2611-3221, 2622-2901, 2630-3250, 2633-2928, 2633-3247, 2653-3220, 2660-2912, 2668-3012, 2676-2969, 2690-3137, 2694-3077, 2722-3240, 2724-3250, 2752-3044, 2754-3215, 2761-2954, 2761-3011, 2776-3249, 2779-3250, 2788-3249, 2791-3041, 2799-3075, 2816-3250, 2821-3250, 2841-3112, 2842-3105, 2843-3070, 2847-3250, 2857-3248, 2859-3246, 2892-3250, 2902-3250, 2922-3217, 2931-3112, 2937-3250, 2952-3250, 2980-3242, 2993-3250, 2994-3244, 2998-3250, 3005-3250, 3008-3249, 3011-3250, 3035-3250, 3045-3250, 3048-3249, 3060-3250, 3074-3250, 3080-3250, 3143-3250, 3165-3250 65/ 1-161, 1-181, 1-239, 1-283, 1-302, 1-343, 1-365, 1-413, 1-448, 1-453, 1-458, 1-484, 1-486, 1-502, 1-509, 1-516, 2122511CB1/ 1-543, 1-561, 1-580, 1-584, 1-586, 11-615, 15-495, 86-458, 135-348, 148-766, 184-667, 303-663, 318-569, 432-676, 1399 446-960, 453-960, 497-726, 530-1047, 559-1142, 599-622, 625-1237, 664-1101, 664-1298, 671-1305, 693-1003, 732-1178, 743-1369, 755-965, 797-1083, 826-1123, 834-1397, 871-1367, 921-1335, 927-1380, 931-1161, 959-1399, 965-1387, 1015-1186, 1086-1358, 1086-1399, 1113-1385, 1216-1399 66/ 1-495, 36-495, 88-1003, 506-1057, 597-1000, 597-1299, 597-1436, 719-926, 819-1462, 883-1502, 1035-1462, 55009131CB1/ 1058-1565, 1316-1502, 1427-1929, 1566-2629, 1585-2017, 1585-2051, 1684-2259, 1684-2276, 1753-2274, 8538 1769-2245, 2288-2543, 2288-2852, 2328-2932, 2335-2577, 2609-3178, 2612-3135, 2642-4056, 2729-3240, 2774-3293, 2775-3364, 2780-3328, 2780-3331, 2807-3361, 2872-3436, 2939-3474, 2963-3600, 2964-3489, 2972-3553, 2981-3503, 2991-3576, 3049-3182, 3049-3185, 3105-3725, 3194-3429, 3209-3433, 3225-3754, 3404-3887, 3433-4058, 3595-3765, 3622-3890, 3891-4087, 3891-4126, 4038-4198, 4053-4198, 4057-5677, 4343-4515, 4352-4515, 4386-4515, 4395-4515, 4425-4515, 4434-4515, 4507-4817, 4507-5003, 4563-5198, 4873-5272, 4915-5517, 5095-5379, 5099-5560, 5126-5722, 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2065-2692, 2069-2857, 2074-2511, 2085-2345, 2094-2337, 2135-2385, 2141-2405, 2141-2849, 2216-2840, 2219-2865, 2243-2854, 2293-2559, 2298-2583, 2308-2870, 2319-2876, 2360-2836, 2368-2499, 2377-2532, 2413-2837, 2463-2696, 2505-2727, 2505-2892, 2589-2819, 2589-3063, 2674-2906, 2694-2847 84/ 1-71, 1-213, 1-275, 3-71, 6-69, 7-71, 7-213, 10-71, 15-209, 20-71, 32-71, 69-166, 69-186, 69-194, 69-203, 69-209, 2300766CB1/ 69-210, 96-656, 172-213, 209-230, 209-251, 209-289, 209-323, 209-382, 210-785, 213-251, 232-504, 235-469, 2512 235-607, 235-683, 243-898, 255-523, 277-756, 296-687, 317-809, 331-940, 340-863, 350-476, 351-425, 351-476, 351-542, 351-583, 351-700, 351-741, 356-535, 361-606, 361-874, 371-755, 406-941, 414-755, 455-723, 462-740, 469-1053, 477-755, 477-1125, 497-1091, 534-756, 554-628, 554-680, 554-977, 565-756, 577-1029, 598-723, 598-729, 600-755, 600-915, 643-938, 664-1029, 714-973, 754-1114, 756-915, 756-1029, 759-1114, 770-1029, 784-1227, 798-965, 799-1602, 807-1050, 811-916, 900-1249, 914-1030, 914-1189, 916-1114, 916-1578, 922-1288, 925-1260, 934-1221, 951-1114, 978-1241, 1030-1219, 1062-1624, 1067-1279, 1067-1552, 1067-1559, 1067-1563, 1067-1614, 1067-1791, 1067-1812, 1067-1877, 1071-1315, 1073-1608, 1075-1351, 1076-1374, 1091-1841, 1103-1369, 1103-1695, 1115-1338, 1170-1431, 1171-1415, 1171-1444, 1184-1811, 1202-1765, 1219-1274, 1219-1338, 1219-1425, 1219-1462, 1219-1520, 1219-1549, 1219-1590, 1219-1602, 1219-1613, 1219-1638, 1219-1686, 1219-1692, 1219-1696, 1219-1777, 1219-1867, 1220-1665, 1227-1844, 1228-1684, 1246-1507, 1259-1872, 1262-1443, 1263-1406, 1265-1777, 1268-1714, 1294-1905, 1299-1554, 1320-1927, 1322-1853, 1325-1891, 1326-1905, 1339-1665, 1341-1722, 1342-1540, 1344-1543, 1363-2182, 1371-1854, 1378-1898, 1387-1658, 1387-1918, 1390-1911, 1400-1929, 1400-2025, 1405-1926, 1424-1884, 1445-1732, 1445-1733, 1449-2252, 1451-1682, 1462-2112, 1477-2226, 1488-1732, 1488-1754, 1491-1760, 1506-1713, 1524-1781, 1529-2189, 1539-2141, 1542-2159, 1543-2211, 1547-2022, 1549-2267, 1556-2183, 1565-1822, 1566-2188, 1582-2512, 1601-1834, 1601-1918, 1601-2124, 1606-2199, 1607-1743, 1608-2194, 1610-2210, 1614-2195, 1617-1886, 1624-1877, 1624-2174, 1627-2226, 1629-2027, 1641-1849, 1641-1858, 1641-2187, 1641-2216, 1654-2226, 1659-2201, 1674-2204, 1688-2320, 1708-1918, 1718-1983, 1720-2211, 1727-2297, 1741-2217, 1743-2300, 1744-2006, 1745-1816, 1745-1886, 1747-2226, 1747-2278, 1750-2220, 1754-2217, 1754-2226, 1763-2217, 1768-2226, 1770-2036, 1770-2037, 1776-2214, 1778-2214, 1779-2226, 1793-2214, 1799-2223, 1801-2181, 1801-2226, 1811-2066, 1812-2029, 1819-2223, 1844-2214, 1846-2217, 1863-2194, 1874-2166, 1874-2194, 1876-2194, 1880-2194, 1880-2219, 1892-2194, 1894-2194, 1897-2194, 1922-2211, 1928-2226, 1938-2293, 1950-2226, 1952-2194, 1965-2194, 1968-2226, 2039-2184, 2067-2193, 2084-2194, 2084-2226, 2087-2194 85/ 1-275, 1-2407, 96-656, 232-504, 235-607, 236-469, 236-683, 243-898, 255-523, 277-756, 296-687, 317-808, 7505816CB1/ 340-863, 351-741, 356-535, 362-606, 362-874, 406-941, 419-1009, 455-536, 455-723, 462-740, 469-1053, 497-1091, 2407 534-756, 643-938, 759-1233, 759-1320, 798-965, 807-1050, 902-1114, 951-1169, 951-1357, 1113-1485, 1113-1864, 1114-1659, 1122-1739, 1142-1402, 1154-1767, 1157-1338, 1161-1672, 1163-1608, 1163-1609, 1196-1449, 1215-1822, 1220-1786, 1221-1799, 1236-1617, 1238-1435, 1239-1438, 1267-1748, 1273-1793, 1274-1781, 1283-1553, 1285-1805, 1295-1921, 1340-1627, 1340-1628, 1344-2147, 1346-1577, 1372-2115, 1383-1627, 1383-1649, 1401-1608, 1404-2095, 1419-1676, 1434-2037, 1445-1918, 1460-1717, 1477-2407, 1496-1729, 1496-1813, 1496-2020, 1501-2095, 1511-2091, 1512-1781, 1519-1772, 1519-2070, 1536-1744, 1536-1753, 1536-1921, 1536-2111, 1549-2115, 1591-2108, 1595-2095, 1603-1813, 1604-2085, 1604-2105, 1607-2121, 1615-1879, 1636-2112, 1640-1781, 1640-1902, 1645-2121, 1645-2123, 1649-2112, 1649-2121, 1658-2112, 1663-2121, 1665-1932, 1671-2109, 1673-2109, 1688-2109, 1694-2118, 1696-2077, 1706-2075, 1707-1962, 1714-2115, 1715-1783, 1739-2109, 1745-2121, 1754-2121, 1758-2090, 1769-2062, 1769-2090, 1771-2090, 1775-2090, 1787-2090, 1789-2090, 1792-2090, 1823-2121, 1845-2121, 1847-2090, 1861-2090, 1864-2121, 1898-2121, 1906-2090, 1935-2080, 1980-2077, 1980-2090, 1980-2121, 2023-2089 86/ 1-69, 1-197, 1-231, 1-1328, 7-137, 18-159, 23-482, 25-124, 27-231, 38-172, 50-231, 53-697, 53-698, 59-698, 7504118CB1/ 230-507, 230-642, 231-659, 233-514, 259-520, 259-571, 272-853, 274-789, 275-920, 277-832, 298-566, 307-581, 1328 313-1021, 323-598, 324-562, 324-719, 345-1200, 346-823, 349-1123, 355-1175, 368-617, 368-638, 373-638, 377-998, 384-669, 406-1140, 447-748, 461-1203, 463-746, 466-794, 467-988, 483-922, 497-884, 518-803, 527-934, 530-998, 532-988, 536-1097, 541-794, 553-808, 562-989, 566-1144, 567-1030, 577-796, 585-853, 586-846, 586-1118, 594-998, 595-1169, 615-1201, 620-1163, 624-1178, 628-1203, 649-1203, 660-1180, 666-1178, 673-884, 675-1238, 680-1203, 704-1266, 722-873, 722-1023, 722-1163, 722-1187, 725-1188, 726-1188, 737-965, 745-1188, 748-1292, 757-1188, 768-1328, 779-1191, 789-1018, 791-1328, 804-1037, 810-1118, 818-1019, 818-1189, 821-1099, 850-1190, 860-1184, 883-1121, 909-1188, 917-1188, 918-1168, 924-1218, 941-1249, 964-1188, 975-1188, 985-1239, 1016-1184, 1026-1301, 1028-1283, 1087-1191, 1105-1308

[0424] TABLE 5 Polynucleotide SEQ ID NO: Incyte Project ID: Representative Library 44 2489747CB1 THYMNOR02 45 5857405CB1 BRAINON01 46 2891329CB1 BRAINOT04 47 7474130CB1 COLNDIS02 48 2109928CB1 PROSNOT15 49 2675716CB1 SCORNOT01 50 1953366CB1 PITUNOT01 51 3992330CB1 ADRETUT06 52 4043652CB1 BRAINOT09 53 5540353CB1 KIDNFEC01 54 5632328CB1 PLACFER01 55 6727209CB1 PROSTMT02 56 6923150CB1 PLACFER06 57 2589084CB1 FIBPNOT01 58 7950559CB1 BRABNOE02 59 6981966CB1 BRAIFER05 60 1287125CB1 BRAENOT02 61 2924950CB1 LIVRNON08 62 3471345CB1 SINTNOR01 63 3615852CB1 ESOGTME01 64 4973984CB1 LUNGFET03 65 2122511CB1 BRSTNOT07 66 55009131CB1  BRAIFEE03 67 1538253CB1 SINTTUT01 68  030658CB1 NEUTLPT01 70 3359663CB1 LUNGTMT03 71 3237418CB1 COLNNOT11 72 2529616CB1 PITUDIR01 73 7475662CB1 BRAINOY02 74 3811024CB1 BRSTNON02 75 1683407CB1 BRAITDR03 76 1319969CB1 BLADNOT04 77 1645034CB1 MUSCNOT07 78 7949783CB1 BRABNOE02 79 1265361CB1 OVARTUT02 80 2645814CB1 BRAIFER05 81  695481CB1 LUNGTUT08 82  699941CB1 COLENOR03 83 1515839CB1 ENDANOT01 84 2300766CB1 SPLNNOT04 85 7505816CB1 PGANNOT03 86 7504118CB1 SINITMT04

[0425] TABLE 6 Library Vector Library Description ADRETUT06 pINCY Library was constructed using RNA isolated from adrenal tumor tissue removed from a 57-year-old Caucasian female during a unilateral right adrenalectomy. Pathology indicated pheochromocytoma, forming a nodular mass completely replacing the medulla of the adrenal gland. BLADNOT04 pINCY Library was constructed using RNA isolated from bladder tissue of a 28-year-old Caucasian male, who died from a self-inflicted gunshot wound. BRABNOE02 PBK-CMV This 5′ biased random primed library was constructed using RNA isolated from vermis tissue removed from a 35-year-old Caucasian male who died from cardiac failure. Pathology indicated moderate leptomeningeal fibrosis and multiple microinfarctions of the cerebral neocortex. Patient history included dilated cardiomyopathy, congestive heart failure, cardiomegaly, and an enlarged spleen and liver. Patient medications included simethicone, Lasix, Digoxin, Colace, Zantac, captopril, and Vasotec. BRAENOT02 pINCY Library was constructed using RNA isolated from posterior parietal cortex tissue removed from the brain of a 35-year-old Caucasian male who died from cardiac failure. BRAIFEE03 pINCY This 5′ biased random primed library was constructed using RNA isolated from brain tissue removed from a Caucasian male fetus who was stillborn with a hypoplastic left heart at 23 weeks' gestation. BRAIFER05 pINCY Library was constructed using RNA isolated from brain tissue removed from a Caucasian male fetus who was stillborn with a hypoplastic left heart at 23 weeks' gestation. BRAINON01 PSPORT1 Library was constructed and normalized from 4.88 million independent clones from a brain tissue library. RNA was made from brain tissue removed from a 26-year-old Caucasian male during cranioplasty and excision of a cerebral meningeal lesion. Pathology for the associated tumor tissue indicated a grade 4 oligoastrocytoma in the right fronto-parietal part of the brain. The normalization and hybridization conditions were adapted from Soares et al., PNAS (1994) 91: 9228, except that a significantly longer (48-hour) reannealing hybridization was used. BRAINOT04 PSPORT1 Library was constructed using RNA isolated from the brain tissue of a 44-year-old Caucasian male with a cerebral hemorrhage. The tissue, which contained coagulated blood, came from the choroid plexus of the right anterior temporal lobe. Family history included coronary artery disease and myocardial infarction. BRAINOT09 pINCY Library was constructed using RNA isolated from brain tissue removed from a Caucasian male fetus, who died at 23 weeks' gestation. BRAINOY02 pINCY This large size-fractionated and normalized library was constructed using pooled cDNA generated using mRNA isolated from midbrain, inferior temporal cortex, medulla, and posterior parietal cortex tissues removed from a 35-year-old Caucasian male who died from cardiac failure. Pathology indicated moderate leptomeningeal fibrosis and multiple microinfarctions of the cerebral neocortex. Microscopically, the cerebral hemisphere revealed moderate fibrosis of the leptomeninges with focal calcifications. There was evidence of shrunken and slightly eosinophilic pyramidal neurons throughout the cerebral hemispheres. Scattered throughout the cerebral cortex, there were multiple small microscopic areas of cavitation with surrounding gliosis. Patient history included dilated cardiomyopathy, congestive heart failure, cardiomegaly and an enlarged spleen and liver. 0.28 million independent clones from this size-selected library were normalized in two rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228-9232 and Bonaldo et al., Genome Research 6 (1996): 791, except that a significantly longer (48 hours/round) reannealing hybridization was used. BRAITDR03 PCDNA2.1 This random primed library was constructed using RNA isolated from allocortex, cingulate posterior tissue removed from a 55-year-old Caucasian female who died from cholangiocarcinoma. Pathology indicated mild meningeal fibrosis predominately over the convexities, scattered axonal spheroids in the white matter of the cingulate cortex and the thalamus, and a few scattered neurofibrillary tangles in the entorhinal cortex and the periaqueductal gray region. Pathology for the associated tumor tissue indicated well- differentiated cholangiocarcinoma of the liver with residual or relapsed tumor. Patient history included cholangiocarcinoma, post-operative Budd-Chiari syndrome, biliary ascites, hydrothorax, dehydration, malnutrition, oliguria and acute renal failure. Previous surgeries included cholecystectomy and resection of 85% of the liver. BRSTNON02 pINCY This normalized breast tissue library was constructed from 6.2 million independent clones from a pool of two libraries from two different donors. Starting RNA was made from breast tissue removed from a 46-year-old Caucasian female during a bilateral reduction mammoplasty (donor A), and from breast tissue removed from a 60-year-old Caucasian female during a bilateral reduction mammoplasty (donor B). Pathology indicated normal breast parenchyma, bilaterally (A) and bilateral mammary hypertrophy (B). Patient history included hypertrophy of breast, obesity, lumbago, and glaucoma (A) and joint pain in the shoulder, thyroid cyst, colon cancer, normal delivery and cervical cancer (B). Family history included cataract, osteoarthritis, uterine cancer, benign hypertension, hyperlipidemia, and alcoholic cirrhosis of the liver, cerebrovascular disease, and type II diabetes (A) and cerebrovascular accident, atherosclerotic coronary artery disease, colon cancer, type II diabetes, hyperlipidemia, depressive disorder, and Alzheimer's Disease. The library was normalized in two rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228-9232 and Bonaldo et al., Genome Research 6 (1996): 791, exce

BRSTNOT07 pINCY Library was constructed using RNA isolated from diseased breast tissue removed from a 43-year-old Caucasian female during a unilateral extended simple mastectomy. Pathology indicated mildly proliferative fibrocystic changes with epithelial hyperplasia, papillomatosis, and duct ectasia. Pathology for the associated tumor tissue indicated invasive grade 4, nuclear grade 3 mammary adenocarcinoma with extensive comedo necrosis. Family history included epilepsy, cardiovascular disease, and type II diabetes. COLENOR03 PCDNA2.1 Library was constructed using RNA isolated from colon epithelium tissue removed from a 13-year-old Caucasian female who died from a motor vehicle accident. COLNDIS02 pINCY This subtracted tissue library was constructed using 4.72 million clones from a diseased colon and colon polyp tissue library and was subjected to 2 rounds of subtraction hybridization with 7 million clones from a pooled normal colon tissue library. The starting library for subtraction was constructed using pooled cDNA from two donors. cDNA was generated using mRNA isolated from diseased colon tissue removed from the cecum and descending colon of a 16-year-old Caucasian male (donor A) during partial colectomy, temporary ileostomy, and colonoscopy and from diseased colon polyp tissue removed from the cecum of a 67-year-old female (donor B). Pathology indicated innumerable (greater than 100) adenomatous polyps with low-grade dysplasia involving the entire colonic mucosa in the setting of familial polyposis coli (A) and a benign cecum polyp (B). Pathology for the associated tumor tissue (B) indicated invasive grade 3 adenocarcinoma that arose in tubulovillous adenoma forming a fungating mass in the cecum. Multiple (2 of 17) regional lymph nodes were involved by metastatic adenocarcinoma. A tubulovillous adenoma and multiple (6) tubular adenomas wit

COLNNOT11 PSPORT1 Library was constructed using RNA isolated from colon tissue removed from a 60-year-old Caucasian male during a left hemicolectomy. ENDANOT01 PBLUESCRIPT Library was constructed using RNA isolated from aortic endothelial cell tissue from an explanted heart removed from a male during a heart transplant. ESOGTME01 PSPORT This 5′ biased random primed library was constructed using RNA isolated from esophageal tissue removed from a 53-year-old Caucasian male during a partial esophagectomy, proximal gastrectomy, and regional lymph node biopsy. Pathology indicated no significant abnormality in the non-neoplastic esophagus. Pathology for the matched tumor tissue indicated invasive grade 4 (of 4) adenocarcinoma, forming a sessile mass situated in the lower esophagus, 2 cm from the gastroesophageal junction and 7 cm from the proximal margin. The tumor invaded through the muscularis propria into the adventitial soft tissue. Metastatic carcinoma was identified in 2 of 5 paragastric lymph nodes with perinodal extension. The patient presented with dysphagia. Patient history included membranous nephritis, hyperlipidemia, benign hypertension, and anxiety state. Previous surgeries included an adenotonsillectomy, appendectomy, and inguinal hernia repair. The patient was not taking any medications. Family history included atherosclerotic coronary artery disease, alcoholic cirrhosis, alcohol abuse, and an abdominal aortic aneurysm rupture in the father; breast cancer in the mother; a myocardial infarction a

FIBPNOT01 pINCY Library was constructed using RNA isolated from fibroblasts of the prostate stroma removed from a male fetus, who died after 26 weeks' gestation. KIDNFEC01 PBLUESCRIPT Library was constructed using RNA isolated from kidney tissue removed from a pool of twelve Caucasian male and female fetuses that were spontaneously aborted at 19-23 weeks' gestation. LIVRNON08 pINCY This normalized library was constructed from 5.7 million independent clones from a pooled liver tissue library. Starting RNA was made from pooled liver tissue removed from a 4-year-old Hispanic male who died from anoxia and a 16 week female fetus who died after 16-weeks gestation from anencephaly. Serologies were positive for cytolomegalovirus in the 4-year-old. Patient history included asthma in the 4-year-old. Family history included taking daily prenatal vitamins and mitral valve prolapse in the mother of the fetus. The library was normalized in 2 rounds using conditions adapted from Soares et al., PNAS (1994) 91: 9228 and Bonaldo et al., Genome Research 6 (1996): 791, except that a significantly longer (48 hours/round) reannealing hybridization was used. LUNGFET03 pINCY Library was constructed using RNA isolated from lung tissue removed from a Caucasian female fetus, who died at 20 weeks' gestation. LUNGTMT03 pINCY Library was constructed using RNA isolated from right lung tissue removed from a 43-year-old Caucasian male during right thoracotomy and bronchoscopy. Pathology for the associated tumor tissue indicated poorly differentiated adenocarcinoma. Grossly, the hilar region revealed a mass, adjacent to the bronchus. Lymph nodes were attached to the mass. Patient history included non-small cell carcinoma, dermatomyositis and tobacco use. Family history included cancer (unspecified site) and hypertension. LUNGTUT08 pINCY Library was constructed using RNA isolated from lung tumor tissue removed from a 63-year-old Caucasian male during a right upper lobectomy with fiberoptic bronchoscopy. Pathology indicated a grade 3 adenocarcinoma. Patient history included atherosclerotic coronary artery disease, an acute myocardial infarction, rectal cancer, an asymtomatic abdominal aortic aneurysm, tobacco abuse, and cardiac dysrhythmia. Family history included congestive heart failure, stomach cancer, and lung cancer, type II diabetes, atherosclerotic coronary artery disease, and an acute myocardial infarction. MUSCNOT07 pINCY Library was constructed using RNA isolated from muscle tissue removed from the forearm of a 38-year-old Caucasian female during a soft tissue excision. Pathology for the associated tumor tissue indicated intramuscular hemangioma. Family history included breast cancer, benign hypertension, cerebrovascular disease, colon cancer, and type II diabetes. NEUTLPT01 PBLUESCRIPT Library was constructed using RNA isolated from peripheral blood granulocytes collected by density gradient centrifugation through Ficoll-Hypaque. The cells were isolated from buffy coat units obtained from unrelated male and female donors. Cells were cultured in 100 ng/ml E. coli LPS for 30 minutes, lysed in GuSCN, and spun through CsCl to obtain RNA for library construction. OVARTUT02 pINCY Library was constructed using RNA isolated from ovarian tumor tissue removed from a 51-year-old Caucasian female during an exploratory laparotomy, total abdominal hysterectomy, salpingo-oophorectomy, and an incidental appendectomy. Pathology indicated mucinous cystadenoma presenting as a multiloculated neoplasm involving the entire left ovary. The right ovary contained a follicular cyst and a hemorrhagic corpus luteum. The uterus showed proliferative endometrium and a single intramural leiomyoma. The peritoneal biopsy indicated benign glandular inclusions consistent with endosalpingiosis. Family history included atherosclerotic coronary artery disease, benign hypertension, breast cancer, and uterine cancer. PGANNOT03 pINCY Library was constructed using RNA isolated from paraganglionic tumor tissue removed from the intra-abdominal region of a 46-year-old Caucasian male during exploratory laparotomy. Pathology indicated a benign paraganglioma and was associated with a grade 2 renal cell carcinoma, clear cell type, which did not penetrate the capsule. Surgical margins were negative for tumor. PITUDIR01 PCDNA2.1 This random primed library was constructed using RNA isolated from pituitary gland tissue removed from a 70-year-old female who died from metastatic adenocarcinoma. PITUNOT01 PBLUESCRIPT Library was constructed using RNA obtained from Clontech (CLON 6584-2, lot 35278). The RNA was isolated from the pituitary glands removed from a pool of 18 male and female Caucasian donors, 16 to 70 years old, who died from trauma. PLACFER01 pINCY The library was constructed using RNA isolated from placental tissue removed from a Caucasian fetus, who died after 16 weeks' gestation from fetal demise and hydrocephalus. Patient history included umbilical cord wrapped around the head (3 times) and the shoulders (1 time). Serology was positive for anti-CMV. Family history included multiple pregnancies and live births, and an abortion. PLACFER06 pINCY This random primed library was constructed using RNA isolated from placental tissue removed from a Caucasian fetus who died after 16 weeks' gestation from fetal demise and hydrocephalus. Patient history included umbilical cord wrapped around the head (3 times) and the shoulders (1 time). Serology was positive for anti-CMV. Family history included multiple pregnancies and live births, and an abortion. PROSNOT15 pINCY Library was constructed using RNA isolated from diseased prostate tissue removed from a 66-year-old Caucasian male during radical prostatectomy and regional lymph node excision. Pathology indicated adenofibromatous hyperplasia. Pathology for the associated tumor tissue indicated an adenocarcinoma (Gleason grade 2 + 3). The patient presented with elevated prostate specific antigen (PSA). Family history included prostate cancer, secondary bone cancer, and benign hypertension. PROSTMT02 pINCY The library was constructed using RNA isolated from diseased prostate tissue removed from a 66-year-old Caucasian male during radical prostatectomy, regional lymph node excision, and prostate needle biopsy. Pathology indicated adenofibromatous hyperplasia. Pathology from the associated tumor indicated adenocarcinoma Gleason grade 3 + 4, forming a predominant mass involving the right lobe and the left side centrally. The patient presented with elevated prostate specific antigen (PSA) and induration. Family history included acute myocardial infarction, atherosclerotic coronary artery disease, type II diabetes, hyperlipidemia, and Jakob-Creutzfeldt disease. SCORNOT01 PSPORT1 Library was constructed using RNA isolated from spinal cord tissue removed from a 71-year-old Caucasian male who died from respiratory arrest. Patient history included myocardial infarction, gangrene, and end stage renal disease. SINITMT04 pINCY Library was constructed using RNA isolated from ileum tissue removed from a 70-year-old Caucasian female during right hemicolectomy, open liver biopsy, flexible sigmoidoscopy, colonoscopy, and permanent colostomy. Pathology for the associated tumor indicated invasive grade 2 adenocarcinoma forming an ulcerated mass, situated 2 cm distal to the ileocecal valve. Patient history included a malignant breast neoplasm, type II diabetes, hyperlipidemia, viral hepatitis, an unspecified thyroid disorder, osteoarthritis, a malignant skin neoplasm, and normal delivery. Family history included breast cancer, atherosclerotic coronary artery disease, benign hypertension, cerebrovascular disease, breast cancer, ovarian cancer, and hyperlipidemia. SINTNOR01 PCDNA2.1 This random primed library was constructed using RNA isolated from small intestine tissue removed from a 31-year-old Caucasian female during Roux-en-Y gastric bypass. Patient history included clinical obesity. SINTTUT01 PSPORT1 Library was constructed using RNA isolated from small intestine tumor tissue obtained from a 42-year-old Caucasian male during a right hemicolectomy and permanent colostomy. Carcinoid tumor was identified in the ileum. Patient history included benign hypertension. Previous surgeries included a cholecystectomy. Family history included benign hypertension, a cerebrovascular accident, malignant neoplasm of prostate, and tuberculosis. SPLNNOT04 pINCY Library was constructed using RNA isolated from the spleen tissue of a 2-year-old Hispanic male, who died from cerebral anoxia. Past medical history and serologies were negative. THYMNOR02 pINCY The library was constructed using RNA isolated from thymus tissue removed from a 2-year-old Caucasian female during a thymectomy and patch closure of left atrioventricular fistula. Pathology indicated there was no gross abnormality of the thymus. The patient presented with congenital heart abnormalities. Patient history included double inlet left ventricle and a rudimentary right ventricle, pulmonary hypertension, cyanosis, subaortic stenosis, seizures, and a fracture of the skull base. Family history included reflux neuropathy.

[0426] TABLE 7 Program Description Reference Parameter Threshold ABI A program that removes vector sequences and Applied Biosystems, Foster City, CA. FACTURA masks ambiguous bases in nucleic acid sequences. ABI/ A Fast Data Finder useful in comparing and Applied Biosystems, Foster City, CA; Mismatch <50% PARACEL annotating amino acid or nucleic acid sequences. Paracel Inc., Pasadena, CA. FDF ABI A program that assembles nucleic acid sequences. Applied Biosystems, Foster City, CA. Auto- Assembler BLAST A Basic Local Alignment Search Tool useful in Altschul, S. F. et al. (1990) J. Mol. Biol. ESTs: Probability value = sequence similarity search for amino acid and 215: 403-410; Altschul, S. F. et al. (1997) 1.0E−8 or less; Full Length nucleic acid sequences. BLAST includes five Nucleic Acids Res. 25: 3389-3402. sequences: Probability functions: blastp, blastn, blastx, tblastn, and tblastx. value = 1.0E−10 or less FASTA A Pearson and Lipman algorithm that searches for Pearson, W. R. and D. J. Lipman (1988) Proc. ESTs: fasta E value = similarity between a query sequence and a group of Natl. Acad Sci. USA 85: 2444-2448; Pearson, 1.06E−6; Assembled sequences of the same type. FASTA comprises as W. R. (1990) Methods Enzymol. 183: 63-98; ESTs: fasta Identity = 95% least five functions: fasta, tfasta, fastx; tfastx, and and Smith, T. F. and M. S. Waterman (1981) or greater and Match ssearch. Adv. Appl. Math. 2: 482-489. length = 200 bases or greater; fastx E value = 1.0E−8 or less; Full Length sequences: fastx score = 100 or greater BLIMPS A BLocks IMProved Searcher that matches a Henikoff, S. and J. G. Henikoff (1991) Probability value = 1.0E−3 sequence against those in BLOCKS, PRINTS, Nucleic Acids Res. 19: 6565-6572; Henikoff, or less DOMO, PRODOM, and PFAM databases to search J. G. and S. Henikoff (1996) Methods for gene families, sequence homology, and structural Enzymol. 266: 88-105; and Attwood, T. K. et fingerprint regions. al. (1997) J. Chem. Inf. Comput. Sci. 37: 417-424. HMMER An algorithm for searching a query sequence against Krogh, A. et al. (1994) J. Mol. Biol. PFAM or SMART hits: hidden Markov model (HMM)-based databases of 235: 1501-1531; Sonnhammer, E. L. L. et al. Probability value = 1.0E−3 protein family consensus sequences, such as PFAM (1988) Nucleic Acids Res. 26: 320-322; or less; Signal peptide and SMART. Durbin, R. et al. (1998) Our World View, in hits: Score = 0 or greater a Nutshell, Cambridge Univ. Press, pp. 1-350. ProfileScan An algorithm that searches for structural and Gribskov, M. et al. (1988) CABIOS 4: 61-66; Normalized quality sequence motifs in protein sequences that match Gribskov, M. et al. (1989) Methods score ≧ GCG-specified sequence patterns defined in Prosite. Enzymol. 183: 146-159; Bairoch, A. et al. “HIGH” value for that (1997) Nucleic Acids Res. 25: 217-221. particular Prosite motif. Generally, score = 1.4-2.1. Phred A base-calling algorithm that examines automated Ewing, B. et al. (1998) Genome Res. 8: 175-185; sequencer traces with high sensitivity and probability. Ewing, B. and P. Green (1998) Genome Res. 8: 186-194. Phrap A Phils Revised Assembly Program including Smith, T. F. and M. S. Waterman (1981) Adv. Score = 120 or greater; SWAT and CrossMatch, programs based on efficient Appl. Math. 2: 482-489; Smith, T. F. and Match length = 56 or implementation of the Smith-Waterman algorithm, M. S. Waterman (1981) J. Mol. Biol. 147: 195-197; greater useful in searching sequence homology and and Green, P., University of assembling DNA sequences. Washington, Seattle, WA. Consed A graphical tool for viewing and editing Phrap Gordon, D. et al. (1998) Genome Res. 8: 195-202. assemblies. SPScan A weight matrix analysis program that scans protein Nielson, H. et al. (1997) Protein Engineering Score = 3.5 or greater sequences for the presence of secretory signal 10: 1-6; Claverie, J. M. and S. Audic (1997) peptides. CABIOS 12: 431-439. TMAP A program that uses weight matrices to delineate Persson, B. and P. Argos (1994) J. Mol. Biol. transmembrane segments on protein sequences and 237: 182-192; Persson, B. and P. Argos determine orientation. (1996) Protein Sci. 5: 363-371. TMHMMER A program that uses a hidden Markov model (HMM) Sonnhammer, E. L. et al. (1998) Proc. Sixth to delineate transmembrane segments on protein Intl. Conf. On Intelligent Systems for Mol. sequences and determine orientation. Biol., Glasgow et al., eds., The Am. Assoc. for Artificial Intelligence (AAAI) Press, Menlo Park, CA, and MIT Press, Cambridge, MA, pp. 175-182. Motifs A program that searches amino acid sequences for Bairoch, A. et al. (1997) Nucleic Acids Res. patterns that matched those defined in Prosite. 25: 217-221; Wisconsin Package Program Manual, version 9, page M51-59, Genetics Computer Group, Madison, WI.

[0427]

0 SEQUENCE LISTING <160> NUMBER OF SEQ ID NOS: 86 <210> SEQ ID NO 1 <211> LENGTH: 1887 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2489747CD1 <400> SEQUENCE: 1 Met Ala Ala Arg Gly Arg Gly Leu Leu Leu Leu Thr Leu Ser Val 1 5 10 15 Leu Leu Ala Ala Gly Pro Ser Ala Ala Ala Ala Lys Leu Asn Ile 20 25 30 Pro Lys Val Leu Leu Pro Phe Thr Arg Ala Thr Arg Val Asn Phe 35 40 45 Thr Leu Glu Ala Ser Glu Gly Cys Tyr Arg Trp Leu Ser Thr Arg 50 55 60 Pro Glu Val Ala Ser Ile Glu Pro Leu Gly Leu Asp Glu Gln Gln 65 70 75 Cys Ser Gln Lys Ala Val Val Gln Ala Arg Leu Thr Gln Pro Ala 80 85 90 Arg Leu Thr Ser Ile Ile Phe Ala Glu Asp Ile Thr Thr Gly Gln 95 100 105 Val Leu Arg Cys Asp Ala Ile Val Asp Leu Ile His Asp Ile Gln 110 115 120 Ile Val Ser Thr Thr Arg Glu Leu Tyr Leu Glu Asp Ser Pro Leu 125 130 135 Glu Leu Lys Ile Gln Ala Leu Asp Ser Glu Gly Asn Thr Phe Ser 140 145 150 Thr Leu Ala Gly Leu Val Phe Glu Trp Thr Ile Val Lys Asp Ser 155 160 165 Glu Ala Asp Arg Phe Ser Asp Ser His Asn Ala Leu Arg Ile Leu 170 175 180 Thr Phe Leu Glu Ser Thr Tyr Ile Pro Pro Ser Tyr Ile Ser Glu 185 190 195 Met Glu Lys Ala Ala Lys Gln Gly Asp Thr Ile Leu Val Ser Gly 200 205 210 Met Lys Thr Gly Ser Ser Lys Leu Lys Ala Arg Ile Gln Glu Ala 215 220 225 Val Tyr Lys Asn Val Arg Pro Ala Glu Val Arg Leu Leu Ile Leu 230 235 240 Glu Asn Ile Leu Leu Asn Pro Ala Tyr Asp Val Tyr Leu Met Val 245 250 255 Gly Thr Ser Ile His Tyr Lys Val Gln Lys Ile Arg Gln Gly Lys 260 265 270 Ile Thr Glu Leu Ser Met Pro Ser Asp Gln Tyr Glu Leu Gln Leu 275 280 285 Gln Asn Ser Ile Pro Gly Pro Glu Gly Asp Pro Thr Arg Pro Val 290 295 300 Ala Val Leu Ala Gln Asp Thr Ser Met Val Thr Ala Leu Gln Leu 305 310 315 Gly Gln Ser Ser Leu Val Leu Gly His Arg Ser Ile Arg Met Gln 320 325 330 Gly Ala Ser Arg Leu Pro Asn Ser Thr Ile Tyr Val Val Glu Pro 335 340 345 Gly Tyr Leu Gly Phe Thr Val His Pro Gly Asp Arg Trp Val Leu 350 355 360 Glu Thr Gly Arg Leu Tyr Glu Ile Thr Ile Glu Val Phe Asp Lys 365 370 375 Phe Ser Asn Lys Val Tyr Val Ser Asp Asn Ile Arg Ile Glu Thr 380 385 390 Val Leu Pro Ala Glu Phe Phe Glu Val Leu Ser Ser Ser Gln Asn 395 400 405 Gly Ser Tyr His Arg Ile Arg Ala Leu Lys Arg Gly Gln Thr Ala 410 415 420 Ile Asp Ala Ala Leu Thr Ser Val Val Asp Gln Asp Gly Gly Val 425 430 435 His Ile Leu Gln Val Pro Val Trp Asn Gln Gln Glu Val Glu Ile 440 445 450 His Ile Pro Ile Thr Leu Tyr Pro Ser Ile Leu Thr Phe Pro Trp 455 460 465 Gln Pro Lys Thr Gly Ala Tyr Gln Tyr Thr Ile Arg Ala His Gly 470 475 480 Gly Ser Gly Asn Phe Ser Trp Ser Ser Ser Ser His Leu Val Ala 485 490 495 Thr Val Thr Val Lys Gly Val Met Thr Thr Gly Ser Asp Ile Gly 500 505 510 Phe Ser Val Ile Gln Ala His Asp Val Gln Asn Pro Leu His Phe 515 520 525 Gly Glu Met Lys Val Tyr Val Ile Glu Pro His Ser Met Glu Phe 530 535 540 Ala Pro Cys Gln Val Glu Ala Arg Val Gly Gln Ala Leu Glu Leu 545 550 555 Pro Leu Arg Ile Ser Gly Leu Met Pro Gly Gly Ala Ser Glu Val 560 565 570 Val Thr Leu Ser Asp Cys Ser His Phe Asp Leu Ala Val Glu Val 575 580 585 Glu Asn Gln Gly Val Phe Gln Pro Leu Pro Gly Arg Leu Pro Pro 590 595 600 Gly Ser Glu His Cys Ser Gly Val Arg Val Lys Ala Glu Ala Gln 605 610 615 Gly Ser Thr Thr Leu Leu Val Ser Tyr Arg His Gly His Val His 620 625 630 Leu Ser Ala Lys Ile Thr Ile Ala Ala Tyr Leu Pro Leu Lys Ala 635 640 645 Val Asp Pro Ser Ser Val Ala Leu Val Thr Leu Gly Ser Ser Lys 650 655 660 Glu Met Leu Phe Glu Gly Gly Pro Arg Pro Trp Ile Leu Glu Pro 665 670 675 Ser Lys Phe Phe Gln Asn Val Thr Ala Glu Asp Thr Asp Ser Ile 680 685 690 Gly Leu Ala Leu Phe Ala Pro His Ser Ser Arg Asn Tyr Gln Gln 695 700 705 His Trp Ile Leu Val Thr Cys Gln Ala Leu Gly Glu Gln Val Ile 710 715 720 Ala Leu Ser Val Gly Asn Lys Pro Ser Leu Thr Asn Pro Phe Pro 725 730 735 Ala Val Glu Pro Ala Val Val Lys Phe Val Cys Ala Pro Pro Ser 740 745 750 Arg Leu Thr Leu Ala Pro Val Tyr Thr Ser Pro Gln Leu Asp Met 755 760 765 Ser Cys Pro Leu Leu Gln Gln Asn Lys Gln Val Val Pro Val Ser 770 775 780 Ser His Arg Asn Pro Leu Leu Asp Leu Ala Ala Tyr Asp Gln Glu 785 790 795 Gly Arg Arg Phe Asp Asn Phe Ser Ser Leu Ser Ile Gln Trp Glu 800 805 810 Ser Thr Arg Pro Val Leu Ala Ser Ile Glu Pro Glu Leu Pro Met 815 820 825 Gln Leu Val Ser Gln Asp Asp Glu Ser Gly Gln Lys Lys Leu His 830 835 840 Gly Leu Gln Ala Ile Leu Val His Glu Ala Ser Gly Thr Thr Ala 845 850 855 Ile Thr Ala Thr Ala Thr Gly Tyr Gln Glu Ser His Leu Ser Ser 860 865 870 Ala Arg Thr Lys Gln Pro His Asp Pro Leu Val Pro Leu Ser Ala 875 880 885 Ser Ile Glu Leu Ile Leu Val Glu Asp Val Arg Val Ser Pro Glu 890 895 900 Glu Val Thr Ile Tyr Asn His Pro Gly Ile Gln Ala Glu Leu Arg 905 910 915 Ile Arg Glu Gly Ser Gly Tyr Phe Phe Leu Asn Thr Ser Thr Ala 920 925 930 Asp Val Val Lys Val Ala Tyr Gln Glu Ala Arg Gly Val Ala Met 935 940 945 Val His Pro Leu Leu Pro Gly Ser Ser Thr Ile Met Ile His Asp 950 955 960 Leu Cys Leu Val Phe Pro Ala Pro Ala Lys Ala Val Val Tyr Val 965 970 975 Ser Asp Ile Gln Glu Leu Tyr Ile Arg Val Val Asp Lys Val Glu 980 985 990 Ile Gly Lys Thr Val Lys Ala Tyr Val Arg Val Leu Asp Leu His 995 1000 1005 Lys Lys Pro Phe Leu Ala Lys Tyr Phe Pro Phe Met Asp Leu Lys 1010 1015 1020 Leu Arg Ala Ala Ser Pro Ile Ile Thr Leu Val Ala Leu Asp Glu 1025 1030 1035 Ala Leu Asp Asn Tyr Thr Ile Thr Phe Leu Ile Arg Gly Val Ala 1040 1045 1050 Ile Gly Gln Thr Ser Leu Thr Ala Ser Val Thr Asn Lys Ala Gly 1055 1060 1065 Gln Arg Ile Asn Ser Ala Pro Gln Gln Ile Glu Val Phe Pro Pro 1070 1075 1080 Phe Arg Leu Met Pro Arg Lys Val Thr Leu Leu Ile Gly Ala Thr 1085 1090 1095 Met Gln Val Thr Ser Glu Gly Gly Pro Gln Pro Gln Ser Asn Ile 1100 1105 1110 Leu Phe Ser Ile Ser Asn Glu Ser Val Ala Leu Val Ser Ala Ala 1115 1120 1125 Gly Leu Val Gln Gly Leu Ala Ile Gly Asn Gly Thr Val Ser Gly 1130 1135 1140 Leu Val Gln Ala Val Asp Ala Glu Thr Gly Lys Val Val Ile Ile 1145 1150 1155 Ser Gln Asp Leu Val Gln Val Glu Val Leu Leu Leu Arg Ala Val 1160 1165 1170 Arg Ile Arg Ala Pro Ile Met Arg Met Arg Thr Gly Thr Gln Met 1175 1180 1185 Pro Ile Tyr Val Thr Gly Ile Thr Asn His Gln Asn Pro Phe Ser 1190 1195 1200 Phe Gly Asn Ala Val Pro Gly Leu Thr Phe His Trp Ser Val Thr 1205 1210 1215 Lys Arg Asp Val Leu Asp Leu Arg Gly Arg His His Glu Ala Ser 1220 1225 1230 Ile Arg Leu Pro Ser Gln Tyr Asn Phe Ala Met Asn Val Leu Gly 1235 1240 1245 Arg Val Lys Gly Arg Thr Gly Leu Arg Val Val Val Lys Ala Val 1250 1255 1260 Asp Pro Thr Ser Gly Gln Leu Tyr Gly Leu Ala Arg Glu Leu Ser 1265 1270 1275 Asp Glu Ile Gln Val Gln Val Phe Glu Lys Leu Gln Leu Leu Asn 1280 1285 1290 Pro Glu Ile Glu Ala Glu Gln Ile Leu Met Ser Pro Asn Ser Tyr 1295 1300 1305 Ile Lys Leu Gln Thr Asn Arg Asp Gly Ala Ala Ser Leu Ser Tyr 1310 1315 1320 Arg Val Leu Asp Gly Pro Glu Lys Val Pro Val Val His Val Asp 1325 1330 1335 Glu Lys Gly Phe Leu Ala Ser Gly Ser Met Ile Gly Thr Ser Thr 1340 1345 1350 Ile Glu Val Ile Ala Gln Glu Pro Phe Gly Ala Asn Gln Thr Ile 1355 1360 1365 Ile Val Ala Val Lys Val Ser Pro Val Ser Tyr Leu Arg Val Ser 1370 1375 1380 Met Ser Pro Val Leu His Thr Gln Asn Lys Glu Ala Leu Val Ala 1385 1390 1395 Val Pro Leu Gly Met Thr Val Thr Phe Thr Val His Phe His Asp 1400 1405 1410 Asn Ser Gly Asp Val Phe His Ala His Ser Ser Val Leu Asn Phe 1415 1420 1425 Ala Thr Asn Arg Asp Asp Phe Val Gln Ile Gly Lys Gly Pro Thr 1430 1435 1440 Asn Asn Thr Cys Val Val Arg Thr Val Ser Val Gly Leu Thr Leu 1445 1450 1455 Leu Arg Val Trp Asp Ala Glu His Pro Gly Leu Ser Asp Phe Met 1460 1465 1470 Pro Leu Pro Val Leu Gln Ala Ile Ser Pro Glu Leu Ser Gly Ala 1475 1480 1485 Met Val Val Gly Asp Val Leu Cys Leu Ala Thr Val Leu Thr Ser 1490 1495 1500 Leu Glu Gly Leu Ser Gly Thr Trp Ser Ser Ser Ala Asn Ser Ile 1505 1510 1515 Leu His Ile Asp Pro Lys Thr Gly Val Ala Val Ala Arg Ala Val 1520 1525 1530 Gly Ser Val Thr Val Tyr Tyr Glu Val Ala Gly His Leu Arg Thr 1535 1540 1545 Tyr Lys Glu Val Val Val Ser Val Pro Gln Arg Ile Met Ala Arg 1550 1555 1560 His Leu His Pro Ile Gln Thr Ser Phe Gln Glu Ala Thr Ala Ser 1565 1570 1575 Lys Val Ile Val Ala Val Gly Asp Arg Ser Ser Asn Leu Arg Gly 1580 1585 1590 Glu Cys Thr Pro Thr Gln Arg Glu Val Ile Gln Ala Leu His Pro 1595 1600 1605 Glu Thr Leu Ile Ser Cys Gln Ser Gln Phe Lys Pro Ala Val Phe 1610 1615 1620 Asp Phe Pro Ser Gln Asp Val Phe Thr Val Glu Pro Gln Phe Asp 1625 1630 1635 Thr Ala Leu Gly Gln Tyr Phe Cys Ser Ile Thr Met His Arg Leu 1640 1645 1650 Thr Asp Lys Gln Arg Lys His Leu Ser Met Lys Lys Thr Ala Leu 1655 1660 1665 Val Val Ser Ala Ser Leu Ser Ser Ser His Phe Ser Thr Glu Gln 1670 1675 1680 Val Gly Ala Glu Val Pro Phe Ser Pro Gly Leu Phe Ala Asp Gln 1685 1690 1695 Ala Glu Ile Leu Leu Ser Asn His Tyr Thr Ser Ser Glu Ile Arg 1700 1705 1710 Val Phe Gly Ala Pro Glu Val Leu Glu Asn Leu Glu Val Lys Ser 1715 1720 1725 Gly Ser Pro Ala Val Leu Ala Phe Ala Lys Glu Lys Ser Phe Gly 1730 1735 1740 Trp Pro Ser Phe Ile Thr Tyr Thr Val Gly Val Leu Asp Pro Ala 1745 1750 1755 Ala Gly Ser Gln Gly Pro Leu Ser Thr Thr Leu Thr Phe Ser Ser 1760 1765 1770 Pro Val Thr Asn Gln Ala Ile Ala Ile Pro Val Thr Val Ala Phe 1775 1780 1785 Val Val Asp Arg Arg Gly Pro Gly Pro Tyr Gly Ala Ser Leu Phe 1790 1795 1800 Gln His Phe Leu Asp Ser Tyr Gln Val Met Phe Phe Thr Leu Phe 1805 1810 1815 Ala Leu Leu Ala Gly Thr Ala Val Met Ile Ile Ala Tyr His Thr 1820 1825 1830 Val Cys Thr Pro Arg Asp Leu Ala Val Pro Ala Ala Leu Thr Pro 1835 1840 1845 Arg Ala Ser Pro Gly His Ser Pro His Tyr Phe Ala Ala Ser Ser 1850 1855 1860 Pro Thr Ser Pro Asn Ala Leu Pro Pro Ala Arg Lys Ala Ser Pro 1865 1870 1875 Pro Ser Gly Leu Trp Ser Pro Ala Tyr Ala Ser His 1880 1885 <210> SEQ ID NO 2 <211> LENGTH: 240 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5857405CD1 <400> SEQUENCE: 2 Met Met Gly Ile Phe Leu Val Tyr Val Gly Phe Val Phe Phe Ser 1 5 10 15 Val Leu Tyr Val Gln Gln Gly Leu Ser Ser Gln Ala Lys Phe Thr 20 25 30 Glu Phe Pro Arg Asn Val Thr Ala Thr Glu Gly Gln Asn Val Glu 35 40 45 Met Ser Cys Ala Phe Gln Ser Gly Ser Ala Ser Val Tyr Leu Glu 50 55 60 Ile Gln Trp Trp Phe Leu Arg Gly Pro Glu Asp Leu Asp Pro Gly 65 70 75 Ala Glu Gly Ala Gly Ala Gln Val Glu Leu Leu Pro Asp Arg Asp 80 85 90 Pro Asp Ser Asp Gly Thr Lys Ile Ser Thr Val Lys Val Gln Gly 95 100 105 Asn Asp Ile Ser His Lys Leu Gln Ile Ser Lys Val Arg Lys Lys 110 115 120 Asp Glu Gly Leu Tyr Glu Cys Arg Val Thr Asp Ala Asn Tyr Gly 125 130 135 Glu Leu Gln Glu His Lys Ala Gln Ala Tyr Leu Lys Val Asn Ala 140 145 150 Asn Ser His Ala Arg Arg Met Gln Ala Phe Glu Ala Ser Pro Met 155 160 165 Trp Leu Gln Asp Met Lys Pro Arg Lys Asn Val Ser Ala Ala Ile 170 175 180 Pro Ser Ser Ile His Gly Ser Ala Asn Gln Arg Thr His Ser Thr 185 190 195 Ser Ser Pro Gln Val Val Ala Lys Ile Pro Lys Gln Ser Pro Gln 200 205 210 Ser Ala Lys Ser Lys Ser Pro Val Lys Ser Thr Glu Arg Thr Ala 215 220 225 Lys Leu Thr Leu Asn Ser Lys His His Pro Ala Pro Thr Val Leu 230 235 240 <210> SEQ ID NO 3 <211> LENGTH: 266 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2891329CD1 <400> SEQUENCE: 3 Met Arg Trp Val Gly Pro Gly Arg Leu Leu Arg Leu Gly Glu Ala 1 5 10 15 Leu Arg Ser Arg Pro Asp Pro Ser Gly Gly Cys Arg Leu Gln Pro 20 25 30 Ala Leu Val Gly Glu Thr Glu Met Ser Glu Lys Glu Asn Asn Phe 35 40 45 Pro Pro Leu Pro Lys Phe Ile Pro Val Lys Pro Cys Phe Tyr Gln 50 55 60 Asn Phe Ser Asp Glu Ile Pro Val Glu His Gln Val Leu Val Lys 65 70 75 Arg Ile Tyr Arg Leu Trp Met Phe Tyr Cys Ala Thr Leu Gly Val 80 85 90 Asn Leu Ile Ala Cys Leu Ala Trp Trp Ile Gly Gly Gly Ser Gly 95 100 105 Thr Asn Phe Gly Leu Ala Phe Val Trp Leu Leu Leu Phe Thr Pro 110 115 120 Cys Gly Tyr Val Cys Trp Phe Arg Pro Val Tyr Lys Ala Phe Arg 125 130 135 Ala Asp Ser Ser Phe Asn Phe Met Ala Phe Phe Phe Ile Phe Gly 140 145 150 Ala Gln Phe Val Leu Thr Val Ile Gln Ala Ile Gly Phe Ser Gly 155 160 165 Trp Gly Ala Cys Gly Trp Leu Ser Ala Ile Gly Phe Phe Gln Tyr 170 175 180 Ser Pro Gly Ala Ala Val Val Met Leu Leu Pro Ala Ile Met Phe 185 190 195 Ser Val Ser Ala Ala Met Met Ala Ile Ala Ile Met Lys Val His 200 205 210 Arg Ile Tyr Arg Gly Ala Gly Gly Ser Phe Gln Lys Ala Gln Thr 215 220 225 Glu Trp Asn Thr Gly Thr Trp Arg Asn Pro Pro Ser Arg Glu Ala 230 235 240 Gln Tyr Asn Asn Phe Ser Gly Asn Ser Leu Pro Glu Tyr Pro Thr 245 250 255 Val Pro Ser Tyr Pro Gly Ser Gly Gln Trp Pro 260 265 <210> SEQ ID NO 4 <211> LENGTH: 824 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7474130CD1 <400> SEQUENCE: 4 Met Lys Ser Ala Lys Pro Gln Val Asn His Ser Gln His Gly Glu 1 5 10 15 Ser Gln Arg Ala Leu Ser Pro Leu Gln Ser Thr Leu Ser Ser Ala 20 25 30 Ala Ser Pro Ser Gln Ala Tyr Glu Thr Tyr Ile Glu Asn Gly Leu 35 40 45 Ile Cys Leu Lys His Lys Ile Arg Asn Ile Glu Lys Lys Lys Leu 50 55 60 Lys Leu Glu Asp Tyr Lys Asp Arg Leu Lys Ser Gly Glu His Leu 65 70 75 Asn Pro Asp Gln Leu Glu Ala Val Glu Lys Tyr Glu Glu Val Leu 80 85 90 His Asn Leu Glu Phe Ala Lys Glu Leu Gln Lys Thr Phe Ser Gly 95 100 105 Leu Ser Leu Asp Leu Leu Lys Ala Gln Lys Lys Ala Gln Arg Arg 110 115 120 Glu His Met Leu Lys Leu Glu Ala Glu Lys Lys Lys Leu Arg Thr 125 130 135 Ile Leu Gln Val Gln Tyr Val Leu Gln Asn Leu Thr Gln Glu His 140 145 150 Val Gln Lys Asp Phe Lys Gly Gly Leu Asn Gly Ala Val Tyr Leu 155 160 165 Pro Ser Lys Glu Leu Asp Tyr Leu Ile Lys Phe Ser Lys Leu Thr 170 175 180 Cys Pro Glu Arg Asn Glu Ser Leu Ser Val Glu Asp Gln Met Glu 185 190 195 Gln Ser Ser Leu Tyr Phe Trp Asp Leu Leu Glu Gly Ser Glu Lys 200 205 210 Ala Val Val Gly Thr Thr Tyr Lys His Leu Lys Asp Leu Leu Ser 215 220 225 Lys Leu Leu Asn Ser Gly Tyr Phe Glu Ser Ile Pro Val Pro Lys 230 235 240 Asn Ala Lys Glu Lys Glu Val Pro Leu Glu Glu Glu Met Leu Ile 245 250 255 Gln Ser Glu Lys Lys Thr Gln Leu Ser Lys Thr Glu Ser Val Lys 260 265 270 Glu Ser Glu Ser Leu Met Glu Phe Ala Gln Pro Glu Ile Gln Pro 275 280 285 Gln Glu Phe Leu Asn Arg Arg Tyr Met Thr Glu Val Asp Tyr Ser 290 295 300 Asn Lys Gln Gly Glu Glu Gln Pro Trp Glu Ala Asp Tyr Ala Arg 305 310 315 Lys Pro Asn Leu Pro Lys Arg Trp Asp Met Leu Thr Glu Pro Asp 320 325 330 Gly Gln Glu Lys Lys Gln Glu Ser Phe Lys Ser Trp Glu Ala Ser 335 340 345 Gly Lys His Gln Glu Val Ser Lys Pro Ala Val Ser Leu Glu Gln 350 355 360 Arg Lys Gln Asp Thr Ser Lys Leu Arg Ser Thr Leu Pro Glu Glu 365 370 375 Gln Lys Lys Gln Glu Ile Ser Lys Ser Lys Pro Ser Pro Ser Gln 380 385 390 Trp Lys Gln Asp Thr Pro Lys Ser Lys Ala Gly Tyr Val Gln Glu 395 400 405 Glu Gln Lys Lys Gln Glu Thr Pro Lys Leu Trp Pro Val Gln Leu 410 415 420 Gln Lys Glu Gln Asp Pro Lys Lys Gln Thr Pro Lys Ser Trp Thr 425 430 435 Pro Ser Val Gln Ser Glu Gln Asn Thr Thr Lys Ser Trp Thr Thr 440 445 450 Pro Met Cys Glu Glu Gln Asp Ser Lys Gln Pro Glu Thr Pro Lys 455 460 465 Ser Trp Glu Asn Asn Val Glu Ser Gln Lys His Ser Leu Thr Ser 470 475 480 Gln Ser Gln Ile Ser Pro Lys Ser Trp Gly Val Ala Thr Ala Ser 485 490 495 Leu Ile Pro Asn Asp Gln Leu Leu Pro Arg Lys Leu Asn Thr Glu 500 505 510 Pro Lys Asp Val Pro Lys Pro Val His Gln Pro Val Gly Ser Ser 515 520 525 Ser Thr Leu Pro Lys Asp Pro Val Leu Arg Lys Glu Lys Leu Gln 530 535 540 Asp Leu Met Thr Gln Ile Gln Gly Thr Cys Asn Phe Met Gln Glu 545 550 555 Ser Val Leu Asp Phe Asp Lys Pro Ser Ser Ala Ile Pro Thr Ser 560 565 570 Gln Pro Pro Ser Ala Thr Pro Gly Ser Pro Val Ala Ser Lys Glu 575 580 585 Gln Asn Leu Ser Ser Gln Ser Asp Phe Leu Gln Glu Pro Leu Gln 590 595 600 Ala Ala Ile Pro Pro Gly Lys Gln Pro Ser Ser Leu Ala Ser Pro 605 610 615 Asn Pro Pro Met Ala Lys Gly Ser Glu Gln Gly Phe Gln Ser Pro 620 625 630 Pro Ala Ser Ser Ser Ser Val Thr Ile Asn Thr Ala Pro Phe Gln 635 640 645 Ala Met Gln Thr Val Phe Asn Val Asn Ala Pro Leu Pro Pro Arg 650 655 660 Lys Glu Gln Glu Ile Lys Glu Ser Pro Tyr Ser Pro Gly Tyr Asn 665 670 675 Gln Ser Phe Thr Thr Ala Ser Thr Gln Thr Pro Pro Gln Cys Gln 680 685 690 Leu Pro Ser Ile His Val Glu Gln Thr Val His Ser Gln Glu Thr 695 700 705 Ala Gln Thr Asn Val Phe Pro Arg Pro Thr Gln Pro Phe Val Asn 710 715 720 Ser Arg Gly Ser Val Arg Gly Cys Thr Arg Gly Gly Arg Leu Ile 725 730 735 Thr Asn Ser Tyr Arg Ser Pro Gly Gly Tyr Lys Gly Phe Asp Thr 740 745 750 Tyr Arg Gly Leu Pro Ser Ile Ser Asn Gly Asn Tyr Ser Gln Leu 755 760 765 Gln Phe Gln Ala Arg Glu Tyr Ser Gly Ala Pro Tyr Ser Gln Arg 770 775 780 Cys Leu Glu Thr Ser Glu Pro Leu Trp Leu Leu Gly Lys Ala Arg 785 790 795 Ile Ile Ser Ser Ser Val Ile Ser Glu Glu Gly His Leu Val Val 800 805 810 His Glu Gln Ile Arg Glu Gln Gly Gly Val Ile Leu Leu Arg 815 820 <210> SEQ ID NO 5 <211> LENGTH: 1026 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2109928CD1 <400> SEQUENCE: 5 Met Glu Gln Leu Ala Asn Ile Ala Met Arg Gln Leu Leu Asp Asn 1 5 10 15 Glu Gly Phe Glu Gln Asp Arg Ser Leu Pro Lys Leu Lys Arg Lys 20 25 30 Ser Pro Lys Lys Val Ser Ala Leu Lys Arg Asp Leu Asp Ala Arg 35 40 45 Ala Lys Ser Glu Arg Tyr Arg Ala Leu Phe Arg Leu Pro Lys Asp 50 55 60 Glu Lys Leu Asp Gly His Thr Asp Cys Thr Leu Trp Thr Pro Phe 65 70 75 Asn Lys Met His Ile Leu Gly Gln Met Phe Val Ser Thr Asn Tyr 80 85 90 Ile Cys Phe Thr Ser Lys Glu Glu Asn Leu Cys Ser Leu Ile Ile 95 100 105 Pro Leu Arg Glu Val Thr Ile Val Glu Lys Ala Asp Ser Ser Ser 110 115 120 Val Leu Pro Ser Pro Leu Ser Ile Ser Thr Arg Asn Arg Met Thr 125 130 135 Phe Leu Phe Ala Asn Leu Lys Asp Arg Asp Phe Leu Val Gln Arg 140 145 150 Ile Ser Asp Phe Leu Gln Gln Thr Thr Ser Lys Ile Tyr Ser Asp 155 160 165 Lys Glu Phe Ala Gly Ser Tyr Asn Ser Ser Asp Asp Glu Val Tyr 170 175 180 Ser Arg Pro Ser Ser Leu Val Ser Ser Ser Pro Gln Arg Ser Thr 185 190 195 Ser Ser Asp Ala Asp Gly Glu Arg Gln Phe Asn Leu Asn Gly Asn 200 205 210 Ser Val Pro Thr Ala Thr Gln Thr Leu Met Thr Met Tyr Arg Arg 215 220 225 Arg Ser Pro Glu Glu Phe Asn Pro Lys Leu Ala Lys Glu Phe Leu 230 235 240 Lys Glu Gln Ala Trp Lys Ile His Phe Ala Glu Tyr Gly Gln Gly 245 250 255 Ile Cys Met Tyr Arg Thr Glu Lys Thr Arg Glu Leu Val Leu Lys 260 265 270 Gly Ile Pro Glu Ser Met Arg Gly Glu Leu Trp Leu Leu Leu Ser 275 280 285 Gly Ala Ile Asn Glu Lys Ala Thr His Pro Gly Tyr Tyr Glu Asp 290 295 300 Leu Val Glu Lys Ser Met Gly Lys Tyr Asn Leu Ala Thr Glu Glu 305 310 315 Ile Glu Arg Asp Leu His Arg Ser Leu Pro Glu His Pro Ala Phe 320 325 330 Gln Asn Glu Met Gly Ile Ala Ala Leu Arg Arg Val Leu Thr Ala 335 340 345 Tyr Ala Phe Arg Asn Pro Asn Ile Gly Tyr Cys Gln Ala Met Asn 350 355 360 Ile Val Thr Ser Val Leu Leu Leu Tyr Ala Lys Glu Glu Glu Ala 365 370 375 Phe Trp Leu Leu Val Ala Leu Cys Glu Arg Met Leu Pro Asp Tyr 380 385 390 Tyr Asn Thr Arg Val Val Gly Ala Leu Val Asp Gln Gly Val Phe 395 400 405 Glu Glu Leu Ala Arg Asp Tyr Val Pro Gln Leu Tyr Asp Cys Met 410 415 420 Gln Asp Leu Gly Val Ile Ser Thr Ile Ser Leu Ser Trp Phe Leu 425 430 435 Thr Leu Phe Leu Ser Val Met Pro Phe Glu Ser Ala Val Val Val 440 445 450 Val Asp Cys Phe Phe Tyr Glu Gly Ile Lys Val Ile Phe Gln Leu 455 460 465 Ala Leu Ala Val Leu Asp Ala Asn Val Asp Lys Leu Leu Asn Cys 470 475 480 Lys Asp Asp Gly Glu Ala Met Thr Val Leu Gly Arg Tyr Leu Asp 485 490 495 Ser Val Thr Asn Lys Asp Ser Thr Leu Pro Pro Ile Pro His Leu 500 505 510 His Ser Leu Leu Ser Asp Asp Val Glu Pro Tyr Pro Glu Val Asp 515 520 525 Ile Phe Arg Leu Ile Arg Thr Ser Tyr Glu Lys Phe Gly Thr Ile 530 535 540 Arg Ala Asp Leu Ile Glu Gln Met Arg Phe Lys Gln Arg Leu Lys 545 550 555 Val Ile Gln Thr Leu Glu Asp Thr Thr Lys Arg Asn Val Val Arg 560 565 570 Thr Ile Val Thr Glu Thr Ser Phe Thr Ile Asp Glu Leu Glu Glu 575 580 585 Leu Tyr Ala Leu Phe Lys Val Ser Cys Lys Ala Glu His Leu Thr 590 595 600 Ser Cys Tyr Trp Gly Gly Ser Ser Asn Ala Leu Asp Arg His Asp 605 610 615 Pro Ser Leu Pro Tyr Leu Glu Gln Tyr Arg Ile Asp Phe Glu Gln 620 625 630 Phe Lys Gly Met Phe Ala Leu Leu Phe Pro Trp Ala Cys Gly Thr 635 640 645 His Ser Asp Val Leu Ala Ser Arg Leu Phe Gln Leu Leu Asp Glu 650 655 660 Asn Gly Asp Ser Leu Ile Asn Phe Arg Glu Phe Val Ser Gly Leu 665 670 675 Ser Ala Ala Cys His Gly Asp Leu Thr Glu Lys Leu Lys Leu Leu 680 685 690 Tyr Lys Met His Val Leu Pro Glu Pro Ser Ser Asp Gln Asp Glu 695 700 705 Pro Asp Ser Ala Phe Glu Ala Thr Gln Tyr Phe Phe Glu Asp Ile 710 715 720 Thr Pro Glu Cys Thr His Val Val Gly Leu Asp Ser Arg Ser Lys 725 730 735 Gln Gly Ala Asp Asp Gly Phe Val Thr Val Ser Leu Lys Pro Asp 740 745 750 Lys Gly Lys Arg Ala Asn Ser Gln Glu Asn Arg Asn Tyr Leu Arg 755 760 765 Leu Trp Thr Pro Glu Asn Lys Ser Lys Ser Lys Asn Ala Lys Asp 770 775 780 Leu Pro Lys Leu Asn Gln Gly Gln Phe Ile Glu Leu Cys Lys Thr 785 790 795 Met Tyr Asn Met Phe Ser Glu Asp Pro Asn Glu Gln Glu Leu Tyr 800 805 810 His Ala Thr Ala Ala Val Thr Ser Leu Leu Leu Glu Ile Gly Glu 815 820 825 Val Gly Lys Leu Phe Val Ala Gln Pro Ala Lys Glu Gly Gly Ser 830 835 840 Gly Gly Ser Gly Pro Ser Cys His Gln Gly Ile Pro Gly Val Leu 845 850 855 Phe Pro Lys Lys Gly Pro Gly Gln Pro Tyr Val Val Glu Ser Val 860 865 870 Glu Pro Leu Pro Ala Ser Leu Ala Pro Asp Ser Glu Glu His Ser 875 880 885 Leu Gly Gly Gln Met Glu Asp Ile Lys Leu Glu Asp Ser Ser Pro 890 895 900 Arg Asp Asn Gly Ala Cys Ser Ser Met Leu Ile Ser Asp Asp Asp 905 910 915 Thr Lys Asp Asp Ser Ser Met Ser Ser Tyr Ser Val Leu Ser Ala 920 925 930 Gly Ser His Glu Glu Asp Lys Leu His Cys Glu Asp Ile Gly Glu 935 940 945 Asp Thr Val Leu Val Arg Ser Gly Gln Gly Thr Ala Ala Leu Pro 950 955 960 Arg Ser Thr Ser Leu Asp Arg Asp Trp Ala Ile Thr Phe Glu Gln 965 970 975 Phe Leu Ala Ser Leu Leu Thr Glu Pro Ala Leu Val Lys Tyr Phe 980 985 990 Asp Lys Pro Val Cys Met Met Ala Arg Ile Thr Ser Ala Lys Asn 995 1000 1005 Ile Arg Met Met Gly Lys Pro Leu Thr Ser Ala Ser Asp Tyr Glu 1010 1015 1020 Ile Ser Ala Met Ser Gly 1025 <210> SEQ ID NO 6 <211> LENGTH: 70 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2675716CD1 <400> SEQUENCE: 6 Met Ala Asn Glu Ser Ser Phe Cys Phe Tyr Phe Leu Ile Phe Leu 1 5 10 15 Gln Cys Leu Cys Ser Gln Phe Ser Trp Phe Ala Phe Phe Phe Phe 20 25 30 Phe Phe Leu Ser Thr Gly Gly Ser Trp Glu Ser Arg Ser His Ala 35 40 45 Ala Cys Gln Glu His Gly Thr Cys Tyr Arg Gly Tyr Ser Pro Ala 50 55 60 Ala Leu Leu Lys Lys Ile Leu Gly Met Ser 65 70 <210> SEQ ID NO 7 <211> LENGTH: 168 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1953366CD1 <400> SEQUENCE: 7 Met Val Arg Ile Gln Arg Arg Lys Leu Leu Ala Ser Cys Leu Cys 1 5 10 15 Val Thr Ala Thr Val Phe Leu Leu Val Thr Leu Gln Val Met Val 20 25 30 Glu Leu Gly Lys Phe Glu Arg Lys Glu Phe Lys Ser Ser Ser Leu 35 40 45 Gln Asp Gly His Thr Lys Met Glu Glu Ala Pro Thr His Leu Asn 50 55 60 Ser Phe Leu Lys Lys Glu Gly Leu Thr Phe Asn Arg Lys Arg Lys 65 70 75 Trp Glu Leu Asp Ser Tyr Pro Ile Met Leu Trp Trp Ser Pro Leu 80 85 90 Thr Gly Glu Thr Gly Arg Leu Gly Gln Cys Gly Ala Asp Ala Cys 95 100 105 Phe Phe Thr Ile Asn Arg Thr Tyr Leu His His His Met Thr Lys 110 115 120 Ala Phe Leu Phe Tyr Gly Leu Thr Thr Gln Lys Met Gly Gly Arg 125 130 135 Arg Tyr Pro Pro Glu Leu Pro Arg Ala His Ser Val Cys Phe Leu 140 145 150 Thr Thr Pro Asp Ser Thr Phe Glu Leu Phe Ala Arg Asp Val Asp 155 160 165 Phe Gln Leu <210> SEQ ID NO 8 <211> LENGTH: 71 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3992330CD1 <400> SEQUENCE: 8 Met Gln Arg Tyr Met Val Leu Leu Val Leu Leu Ile Ile Gln Ile 1 5 10 15 Thr Leu Phe Ala Ser Lys Thr Phe Tyr Leu Ile Ser Leu Leu Asn 20 25 30 Ile Lys Pro Thr Lys Tyr Asn Ser Thr Phe Ser Phe Leu Phe Ser 35 40 45 Phe Gly Ser Tyr Ile Leu Thr Cys Leu Cys Ile Leu Ile Asn Thr 50 55 60 Thr Gly Thr Lys Ile Val Leu Leu Ser Cys Ile 65 70 <210> SEQ ID NO 9 <211> LENGTH: 126 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 4043652CD1 <400> SEQUENCE: 9 Met Phe Asp Ser Ser Val Phe Ser Pro Phe Leu Gly Leu Leu Ala 1 5 10 15 Asn Ala Gln Ala Leu His Phe His Ala Val Leu Ser Ser Leu Trp 20 25 30 Ser Ala Trp Gly Met Val Cys Ser Gln Pro Ala Val Phe Gly Ala 35 40 45 Arg Leu Leu Pro Val Pro Trp Val Leu Glu Leu Glu Glu Ala Val 50 55 60 Leu Ser Pro Phe Pro Phe Leu Lys Ala Val Pro Gly Arg Ala Ser 65 70 75 Gln Gly Arg Arg Arg Gly Leu Arg Val Ser Pro Pro Pro Leu Pro 80 85 90 Phe His Pro Gln Ser Ser Leu Gly Asn Pro Thr Pro Gly Arg Asp 95 100 105 Glu Ala Pro Ser Cys Ser Ala Cys Ser Ala Phe Ser Glu Pro Leu 110 115 120 Gln Gly Ser Ala Asp Ser 125 <210> SEQ ID NO 10 <211> LENGTH: 91 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5540353CD1 <400> SEQUENCE: 10 Met Asp Met Lys Gly Arg Gly Leu Ser Arg Leu Lys Ala Leu Pro 1 5 10 15 Pro Pro Leu Trp Arg Ile Leu Gly Ser Leu Leu Ala Thr Asn Leu 20 25 30 Gly Ser Phe Ser Arg Ser Asp Ala Leu Pro Glu Ile Leu Arg Leu 35 40 45 Val Ser Phe Pro Pro Leu Phe Leu Leu Pro Ile Ser Pro Ser Gln 50 55 60 Gly Ser Glu Leu Pro Pro Gly Arg Leu Gly Leu Asn Trp Leu Leu 65 70 75 Leu Trp Pro Ser Ile Val Ser His Lys Glu Pro Gly Thr Gln His 80 85 90 Val <210> SEQ ID NO 11 <211> LENGTH: 73 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5632328CD1 <400> SEQUENCE: 11 Met Pro Thr Trp Pro Pro Gln Ala Leu Phe Gly Ala Ser Pro Leu 1 5 10 15 Val Leu Val Thr Thr Val Ala Leu Pro Gln His Val Leu Val Thr 20 25 30 Val Leu Phe Pro Ala Asn Leu Trp Arg Ala Arg Thr Val Phe Cys 35 40 45 Ser Phe Ser His Pro His Gly Pro Gln Cys Leu Ala Pro Gly Arg 50 55 60 Cys Pro Ile Asp Val Cys Tyr Thr Lys Arg Ala Gly Glu 65 70 <210> SEQ ID NO 12 <211> LENGTH: 96 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6727209CD1 <400> SEQUENCE: 12 Met Ser Ile Pro Met Val Ser Val Leu Leu Cys Gln Ala Pro Leu 1 5 10 15 Leu Ile Gln Val Ala Leu Pro Arg Thr Val Ala Ile Arg Lys Lys 20 25 30 Arg Leu Cys Leu Val Asp Ser Ile Leu Gln Thr Trp His Leu Phe 35 40 45 Asn Phe Phe Leu Val Gly Phe Ile Phe Gln Ser Ile Phe Arg Phe 50 55 60 Thr Ala Lys Leu Ser Glu Ser Thr Glu Ile Ser His Leu Phe Phe 65 70 75 Ala Pro Thr His Ala Lys Pro His Leu Leu Pro Ile Ser Pro Thr 80 85 90 Arg Glu Val His Leu Leu 95 <210> SEQ ID NO 13 <211> LENGTH: 89 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6923150CD1 <400> SEQUENCE: 13 Met Leu Thr Leu Arg Thr Leu Ala Gly Ser Cys Leu Trp Leu Ser 1 5 10 15 His Leu Val Ser Ser Val Lys Leu Leu Leu Pro Val Gly Asp Val 20 25 30 Val Ile Cys Cys Trp Leu Leu Leu Ile Leu Leu Phe Val Tyr Lys 35 40 45 Val Phe Phe Pro Pro Ser Ala Ser Gln Cys Arg His Arg Phe Met 50 55 60 His Ser Glu Val Val Gly Cys Lys Lys Pro Cys Lys Ala Gly Ser 65 70 75 Ser Leu Leu Asn Ala Ile Ile Tyr Pro Ile Ile Leu Leu Thr 80 85 <210> SEQ ID NO 14 <211> LENGTH: 112 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2589084CD1 <400> SEQUENCE: 14 Met Leu Tyr Lys Ser Asn Lys Leu Lys Ser Pro Ala Ala Glu Arg 1 5 10 15 Arg Thr Glu Glu Thr Arg Ala Val Lys Phe Ile Pro Ser Gln Trp 20 25 30 Ala Ala Met Arg Ser Glu Ser Gln Ser Pro Leu Leu Gln Leu Pro 35 40 45 His Leu Ser Met Gly Leu Ala Asn Leu Ser Thr Gln Arg Met Gly 50 55 60 Arg Arg Thr Gly Trp Gly Ser Thr Trp Lys Asn Gln Gly Gly Gln 65 70 75 Thr Pro Gln Ser Tyr Ser Cys Arg Thr Gly Glu Gly His Gly Pro 80 85 90 Arg Ala Ser Trp Lys Thr Ser Gly His Gly Pro Leu Phe Val Cys 95 100 105 Trp Cys Gln Gly Gly Val Ser 110 <210> SEQ ID NO 15 <211> LENGTH: 73 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7950559CD1 <400> SEQUENCE: 15 Met Asn Met Leu Leu Ile Glu Asp Leu Ser Tyr Leu Ile Met Tyr 1 5 10 15 Leu Gln Ile Phe Ile Ala Leu Ser Phe Leu Leu Leu His Pro Gln 20 25 30 Ile Leu Ile Ser Phe Phe Lys Lys Leu Thr Ser Ser Tyr Val Leu 35 40 45 Ile Ser Phe Thr Leu Leu Lys Pro Val Ser Tyr Thr Ser Asn Val 50 55 60 Gly Leu Leu Ser Pro Gln Leu Leu Pro Arg Trp Thr Ile 65 70 <210> SEQ ID NO 16 <211> LENGTH: 102 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6981966CD1 <400> SEQUENCE: 16 Met Lys Leu Glu Ile Leu Ser Phe Ser Val Leu Asn Leu Leu Ser 1 5 10 15 Cys Ala Ile Leu Phe Leu Val Gln Lys Tyr Thr Ser Pro Cys Lys 20 25 30 Ile Lys Asn Val Ile Ile Pro Asp Lys Asn Phe Lys Leu Cys Ser 35 40 45 Met Lys Ser Trp Ser Trp Ser Asn Ser Leu Lys Arg Phe Ile Glu 50 55 60 Ile Gln Gly Gly His Glu Arg His Ala Leu Thr Pro Pro Thr Trp 65 70 75 Gly Ala Asp Ala Asp Thr Glu Ser Tyr Val Gly Ala Arg Lys Ile 80 85 90 Asn Cys Val Leu Arg Phe Gly Lys Leu Glu Val Val 95 100 <210> SEQ ID NO 17 <211> LENGTH: 96 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1287125CD1 <400> SEQUENCE: 17 Met Ser Arg Thr Gly Leu Val Cys Lys Ser Asp Gln Ile Leu Cys 1 5 10 15 Ala Phe Ile Ser Gln Asp Lys Ala Asn Ser Ser Met Trp Pro Thr 20 25 30 Arg Leu Cys Gly Leu Ala His Leu Pro Phe Gln His Leu Pro Pro 35 40 45 Tyr Ser Leu Tyr Pro Ser Tyr Leu Gly Leu Leu Phe Thr Met Leu 50 55 60 Pro Pro Thr Arg Gly Leu Cys Met Phe Ser Leu Pro Arg Met Phe 65 70 75 Ser Leu Leu Pro Phe Thr Trp Phe Thr Leu Met Leu Gly Asp Arg 80 85 90 Asn Ser Phe Asn Pro Ser 95 <210> SEQ ID NO 18 <211> LENGTH: 305 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2924950CD1 <400> SEQUENCE: 18 Met Ala Ala Gly Leu Ala Arg Leu Leu Leu Leu Leu Gly Leu Ser 1 5 10 15 Ala Gly Gly Pro Ala Pro Ala Gly Ala Ala Lys Met Lys Val Val 20 25 30 Glu Glu Pro Asn Ala Phe Gly Val Asn Asn Pro Phe Leu Pro Gln 35 40 45 Ala Ser Arg Leu Gln Ala Lys Arg Asp Pro Ser Pro Val Ser Gly 50 55 60 Pro Val His Leu Phe Arg Leu Ser Gly Lys Cys Phe Ser Leu Val 65 70 75 Glu Ser Thr Tyr Lys Tyr Glu Phe Cys Pro Phe His Asn Val Thr 80 85 90 Gln His Glu Gln Thr Phe Arg Trp Asn Ala Tyr Ser Gly Ile Leu 95 100 105 Gly Ile Trp His Glu Trp Glu Ile Ala Asn Asn Thr Phe Thr Gly 110 115 120 Met Trp Met Arg Asp Gly Asp Ala Cys Arg Ser Arg Ser Arg Gln 125 130 135 Ser Lys Val Glu Leu Ala Cys Gly Lys Ser Asn Arg Leu Ala His 140 145 150 Val Ser Glu Pro Ser Thr Cys Val Tyr Ala Leu Thr Phe Glu Thr 155 160 165 Pro Leu Val Cys His Pro His Ala Leu Leu Val Tyr Pro Thr Leu 170 175 180 Pro Glu Ala Leu Gln Arg Gln Trp Asp Gln Val Glu Gln Asp Leu 185 190 195 Ala Asp Glu Leu Ile Thr Pro Gln Gly His Glu Lys Leu Leu Arg 200 205 210 Thr Leu Phe Glu Asp Ala Gly Tyr Leu Lys Thr Pro Glu Glu Asn 215 220 225 Glu Pro Thr Gln Leu Glu Gly Gly Pro Asp Ser Leu Gly Phe Glu 230 235 240 Thr Leu Glu Asn Cys Arg Lys Ala His Lys Glu Leu Ser Lys Glu 245 250 255 Ile Lys Arg Leu Lys Gly Leu Leu Thr Gln His Gly Ile Pro Tyr 260 265 270 Thr Arg Pro Thr Glu Thr Ser Asn Leu Glu His Leu Gly His Glu 275 280 285 Thr Pro Arg Ala Lys Ser Pro Glu Gln Leu Arg Gly Asp Pro Gly 290 295 300 Leu Arg Gly Ser Leu 305 <210> SEQ ID NO 19 <211> LENGTH: 144 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3471345CD1 <400> SEQUENCE: 19 Met Phe Arg Glu Gln Pro Val Asp Glu Ile Arg Asn Tyr Phe Gly 1 5 10 15 Glu Lys Val Ala Leu Tyr Phe Val Trp Leu Gly Trp Tyr Thr Tyr 20 25 30 Met Leu Val Pro Ala Ala Leu Thr Gly Leu Leu Val Phe Leu Ser 35 40 45 Gly Phe Ser Leu Phe Glu Ala Ser Gln Ile Ser Lys Glu Ile Cys 50 55 60 Glu Ala His Asp Ile Leu Met Cys Pro Leu Gly Asp His Ser Arg 65 70 75 Arg Tyr Gln Arg Leu Ser Glu Thr Cys Thr Phe Ala Lys Leu Thr 80 85 90 His Leu Phe Asp Asn Asp Gly Thr Val Val Phe Ala Ile Phe Met 95 100 105 Ala Leu Trp Ala Thr Val Phe Leu Glu Ile Trp Lys Arg Gln Arg 110 115 120 Ala Arg Val Val Leu His Trp Asp Leu Tyr Val Trp Asp Glu Glu 125 130 135 Gln Val Arg Trp Ser Trp Gln Arg Ser 140 <210> SEQ ID NO 20 <211> LENGTH: 434 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3615852CD1 <400> SEQUENCE: 20 Met Ser Arg Ser Arg His Leu Gly Lys Ile Arg Lys Arg Leu Glu 1 5 10 15 Asp Val Lys Ser Gln Trp Val Arg Pro Ala Arg Ala Asp Phe Ser 20 25 30 Asp Asn Glu Ser Ala Arg Leu Ala Thr Asp Ala Leu Leu Asp Gly 35 40 45 Gly Ser Glu Ala Tyr Trp Arg Val Leu Ser Gln Glu Gly Glu Val 50 55 60 Asp Phe Leu Ser Ser Val Glu Ala Gln Tyr Ile Gln Ala Gln Ala 65 70 75 Arg Glu Pro Pro Cys Pro Pro Asp Thr Leu Gly Gly Ala Glu Ala 80 85 90 Gly Pro Lys Gly Leu Asp Ser Ser Ser Leu Gln Ser Gly Thr Tyr 95 100 105 Phe Pro Val Ala Ser Glu Gly Ser Glu Pro Ala Leu Leu His Ser 110 115 120 Trp Ala Ser Ala Glu Lys Pro Tyr Leu Lys Glu Lys Ser Ser Ala 125 130 135 Thr Val Tyr Phe Gln Thr Val Lys His Asn Asn Ile Arg Asp Leu 140 145 150 Val Arg Arg Cys Ile Thr Arg Thr Ser Gln Val Leu Val Ile Leu 155 160 165 Met Asp Val Phe Thr Asp Val Glu Ile Phe Cys Asp Ile Leu Glu 170 175 180 Ala Ala Asn Lys Arg Gly Val Phe Val Cys Val Leu Leu Asp Gln 185 190 195 Gly Gly Val Lys Leu Phe Gln Glu Met Cys Asp Lys Val Gln Ile 200 205 210 Ser Asp Ser His Leu Lys Asn Ile Ser Ile Arg Ser Val Glu Gly 215 220 225 Glu Ile Tyr Cys Ala Lys Ser Gly Arg Lys Phe Ala Gly Gln Ile 230 235 240 Arg Glu Lys Phe Ile Ile Ser Asp Trp Arg Phe Val Leu Ser Gly 245 250 255 Ser Tyr Ser Phe Thr Trp Leu Cys Gly His Val His Arg Asn Ile 260 265 270 Leu Ser Lys Phe Thr Gly Gln Ala Val Glu Leu Phe Asp Glu Glu 275 280 285 Phe Arg His Leu Tyr Ala Ser Ser Lys Pro Val Met Gly Leu Lys 290 295 300 Ser Pro Arg Leu Val Ala Pro Val Pro Pro Gly Ala Ala Pro Ala 305 310 315 Asn Gly Arg Leu Ser Ser Ser Ser Gly Ser Ala Ser Asp Arg Thr 320 325 330 Ser Ser Asn Pro Phe Ser Gly Arg Ser Ala Gly Ser His Pro Gly 335 340 345 Thr Arg Ser Val Ser Ala Ser Ser Gly Pro Cys Ser Pro Ala Ala 350 355 360 Pro His Pro Pro Pro Pro Pro Arg Phe Gln Pro His Gln Gly Pro 365 370 375 Trp Gly Ala Pro Ser Pro Gln Ala His Leu Ser Pro Arg Pro His 380 385 390 Asp Gly Pro Pro Ala Ala Val Tyr Ser Asn Leu Gly Ala Tyr Arg 395 400 405 Pro Thr Arg Leu Gln Leu Glu Gln Leu Gly Leu Val Pro Arg Leu 410 415 420 Thr Pro Thr Trp Arg Pro Phe Leu Gln Ala Ser Pro His Phe 425 430 <210> SEQ ID NO 21 <211> LENGTH: 845 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 4973984CD1 <400> SEQUENCE: 21 Met Ser Gly Ala Arg Gly Glu Gly Pro Glu Ala Gly Ala Gly Gly 1 5 10 15 Ala Gly Gly Arg Ala Ala Pro Glu Asn Pro Gly Gly Val Leu Ser 20 25 30 Val Glu Leu Pro Gly Leu Leu Ala Gln Leu Ala Arg Ser Phe Ala 35 40 45 Leu Leu Leu Pro Val Tyr Ala Leu Gly Tyr Leu Gly Leu Ser Phe 50 55 60 Ser Trp Val Leu Leu Ala Leu Ala Leu Leu Ala Trp Cys Arg Arg 65 70 75 Ser Arg Gly Leu Lys Ala Leu Arg Leu Cys Arg Ala Leu Ala Leu 80 85 90 Leu Glu Asp Glu Glu Arg Val Val Arg Leu Gly Val Arg Ala Cys 95 100 105 Asp Leu Pro Ala Trp Val His Phe Pro Asp Thr Glu Arg Ala Glu 110 115 120 Trp Leu Asn Lys Thr Val Lys His Met Trp Pro Phe Ile Cys Gln 125 130 135 Phe Ile Glu Lys Leu Phe Arg Glu Thr Ile Glu Pro Ala Val Arg 140 145 150 Gly Ala Asn Thr His Leu Ser Thr Phe Ser Phe Thr Lys Val Asp 155 160 165 Val Gly Gln Gln Pro Leu Arg Ile Asn Gly Val Lys Val Tyr Thr 170 175 180 Glu Asn Val Asp Lys Arg Gln Ile Ile Leu Asp Leu Gln Ile Ser 185 190 195 Phe Val Gly Asn Cys Glu Ile Asp Leu Glu Ile Lys Arg Tyr Phe 200 205 210 Cys Arg Ala Gly Val Lys Ser Ile Gln Ile His Gly Thr Met Arg 215 220 225 Val Ile Leu Glu Pro Leu Ile Gly Asp Met Pro Leu Val Gly Ala 230 235 240 Leu Ser Ile Phe Phe Leu Arg Lys Pro Leu Leu Glu Ile Asn Trp 245 250 255 Thr Gly Leu Thr Asn Leu Leu Asp Val Pro Gly Leu Asn Gly Leu 260 265 270 Ser Asp Thr Ile Ile Leu Asp Ile Ile Ser Asn Tyr Leu Val Leu 275 280 285 Pro Asn Arg Ile Thr Val Pro Leu Val Ser Glu Val Gln Ile Ala 290 295 300 Gln Leu Arg Phe Pro Val Pro Lys Gly Val Leu Arg Ile His Phe 305 310 315 Ile Glu Ala Gln Asp Leu Gln Gly Lys Asp Thr Tyr Leu Lys Gly 320 325 330 Leu Val Lys Gly Lys Ser Asp Pro Tyr Gly Ile Ile Arg Val Gly 335 340 345 Asn Gln Ile Phe Gln Ser Arg Val Ile Lys Glu Asn Leu Ser Pro 350 355 360 Lys Trp Asn Glu Val Tyr Glu Ala Leu Val Tyr Glu His Pro Gly 365 370 375 Gln Glu Leu Glu Ile Glu Leu Phe Asp Glu Asp Pro Asp Lys Asp 380 385 390 Asp Phe Leu Gly Ser Leu Met Ile Asp Leu Ile Glu Val Glu Lys 395 400 405 Glu Arg Leu Leu Asp Glu Trp Phe Thr Leu Asp Glu Val Pro Lys 410 415 420 Gly Lys Leu His Leu Arg Leu Glu Trp Leu Thr Leu Met Pro Asn 425 430 435 Ala Ser Asn Leu Asp Lys Val Leu Thr Asp Ile Lys Ala Asp Lys 440 445 450 Asp Gln Ala Asn Asp Gly Leu Ser Ser Ala Leu Leu Ile Leu Tyr 455 460 465 Leu Asp Ser Ala Arg Asn Leu Pro Ser Gly Lys Lys Ile Ser Ser 470 475 480 Asn Pro Asn Pro Val Val Gln Met Ser Val Gly His Lys Ala Gln 485 490 495 Glu Ser Lys Ile Arg Tyr Lys Thr Asn Glu Pro Val Trp Glu Glu 500 505 510 Asn Phe Thr Phe Phe Ile His Asn Pro Lys Arg Gln Asp Leu Glu 515 520 525 Val Glu Val Arg Asp Glu Gln His Gln Cys Ser Leu Gly Asn Leu 530 535 540 Lys Val Pro Leu Ser Gln Leu Leu Thr Ser Glu Asp Met Thr Val 545 550 555 Ser Gln Arg Phe Gln Leu Ser Asn Ser Gly Pro Asn Ser Thr Ile 560 565 570 Lys Met Lys Ile Ala Leu Arg Val Leu His Leu Glu Lys Arg Glu 575 580 585 Arg Pro Pro Asp His Gln His Ser Ala Gln Val Lys Arg Pro Ser 590 595 600 Val Ser Lys Glu Gly Arg Lys Thr Ser Ile Lys Ser His Met Ser 605 610 615 Gly Ser Pro Gly Pro Gly Gly Ser Asn Thr Ala Pro Ser Thr Pro 620 625 630 Val Ile Gly Gly Ser Asp Lys Pro Gly Met Glu Glu Lys Ala Gln 635 640 645 Pro Pro Glu Ala Gly Pro Gln Gly Leu His Asp Leu Gly Arg Ser 650 655 660 Ser Ser Ser Leu Leu Ala Ser Pro Gly His Ile Ser Val Lys Glu 665 670 675 Pro Thr Pro Ser Ile Ala Ser Asp Ile Ser Leu Pro Ile Ala Thr 680 685 690 Gln Glu Leu Arg Gln Arg Leu Arg Gln Leu Glu Asn Gly Thr Thr 695 700 705 Leu Gly Gln Ser Pro Leu Gly Gln Ile Gln Leu Thr Ile Arg His 710 715 720 Ser Ser Gln Arg Asn Lys Leu Ile Val Val Val His Ala Cys Arg 725 730 735 Asn Leu Ile Ala Phe Ser Glu Asp Gly Ser Asp Pro Tyr Val Arg 740 745 750 Met Tyr Leu Leu Pro Asp Lys Arg Arg Ser Gly Arg Arg Lys Thr 755 760 765 His Val Ser Lys Lys Thr Leu Asn Pro Val Phe Asp Gln Ser Phe 770 775 780 Asp Phe Ser Val Ser Leu Pro Glu Val Gln Arg Arg Thr Leu Asp 785 790 795 Val Ala Val Lys Asn Ser Gly Gly Phe Leu Ser Lys Asp Lys Gly 800 805 810 Leu Leu Gly Lys Val Leu Val Ala Leu Ala Ser Glu Glu Leu Ala 815 820 825 Lys Gly Trp Thr Gln Trp Tyr Asp Leu Thr Glu Asp Gly Thr Arg 830 835 840 Pro Gln Ala Met Thr 845 <210> SEQ ID NO 22 <211> LENGTH: 270 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2122511CD1 <400> SEQUENCE: 22 Met Val Thr Ala Met Asn Val Ser His Glu Val Asn Gln Leu Phe 1 5 10 15 Gln Pro Tyr Asn Phe Glu Leu Ser Lys Asp Met Arg Pro Phe Phe 20 25 30 Glu Glu Tyr Trp Ala Thr Ser Phe Pro Ile Ala Leu Ile Tyr Leu 35 40 45 Val Leu Ile Ala Val Gly Gln Asn Tyr Met Lys Glu Arg Lys Gly 50 55 60 Phe Asn Leu Gln Gly Pro Leu Ile Leu Trp Ser Phe Cys Leu Ala 65 70 75 Ile Phe Ser Ile Leu Gly Ala Val Arg Met Trp Gly Ile Met Gly 80 85 90 Thr Val Leu Leu Thr Gly Gly Leu Lys Gln Thr Val Cys Phe Ile 95 100 105 Asn Phe Ile Asp Asn Ser Thr Val Lys Phe Trp Ser Trp Val Phe 110 115 120 Leu Leu Ser Lys Val Ile Glu Leu Gly Asp Thr Ala Phe Ile Ile 125 130 135 Leu Arg Lys Arg Pro Leu Ile Phe Ile His Trp Tyr His His Ser 140 145 150 Thr Val Leu Val Tyr Thr Ser Phe Gly Tyr Lys Asn Lys Val Pro 155 160 165 Ala Gly Gly Trp Phe Val Thr Met Asn Phe Gly Val His Ala Ile 170 175 180 Met Tyr Thr Tyr Tyr Thr Leu Lys Ala Ala Asn Val Lys Pro Pro 185 190 195 Lys Met Leu Pro Met Leu Ile Thr Ser Leu Gln Ile Leu Gln Met 200 205 210 Phe Val Gly Ala Ile Val Ser Ile Leu Thr Tyr Ile Trp Arg Gln 215 220 225 Asp Gln Gly Cys His Thr Thr Met Glu His Leu Phe Trp Ser Phe 230 235 240 Ile Leu Tyr Met Thr Tyr Phe Ile Leu Phe Ala His Phe Phe Cys 245 250 255 Gln Thr Tyr Ile Arg Pro Lys Val Lys Ala Lys Thr Lys Ser Gln 260 265 270 <210> SEQ ID NO 23 <211> LENGTH: 2481 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 55009131CD1 <400> SEQUENCE: 23 Met Glu Gln Ser Pro Pro Pro Ala Pro Glu Pro Thr Gln Gly Pro 1 5 10 15 Thr Pro Ala Arg Ser Arg Arg Arg Arg Glu Pro Glu Ser Pro Pro 20 25 30 Ala Ser Ala Pro Ile Pro Leu Phe Gly Ala Asp Thr Ile Gly Gln 35 40 45 Arg Ser Pro Asp Gly Pro Val Leu Ser Lys Ala Glu Phe Val Glu 50 55 60 Lys Val Arg Gln Ser Asn Gln Ala Cys His Asp Gly Asp Phe His 65 70 75 Thr Ala Ile Val Leu Tyr Asn Glu Ala Leu Ala Val Asp Pro Gln 80 85 90 Asn Cys Ile Leu Tyr Ser Asn Arg Ser Ala Ala Tyr Met Lys Ile 95 100 105 Gln Gln Tyr Asp Lys Ala Leu Asp Asp Ala Ile Lys Ala Arg Leu 110 115 120 Leu Asn Pro Lys Trp Pro Lys Ala Tyr Phe Arg Gln Gly Val Ala 125 130 135 Leu Gln Tyr Leu Gly Arg His Ala Asp Ala Leu Ala Ala Phe Ala 140 145 150 Ser Gly Leu Ala Gln Asp Pro Lys Ser Leu Gln Leu Leu Val Gly 155 160 165 Met Val Glu Ala Ala Met Lys Ser Pro Met Arg Asp Ser Leu Glu 170 175 180 Pro Thr Tyr Gln Gln Leu Gln Lys Met Lys Leu Asp Lys Ser Pro 185 190 195 Phe Val Val Val Ser Val Val Gly Gln Glu Leu Leu Thr Ala Gly 200 205 210 His His Gly Ala Ser Val Val Val Leu Glu Ala Ala Leu Lys Ile 215 220 225 Gly Thr Cys Ser Leu Lys Leu Arg Gly Ser Val Phe Ser Ala Leu 230 235 240 Ser Ser Ala Tyr Trp Ser Leu Gly Asn Thr Glu Lys Ser Thr Gly 245 250 255 Tyr Met Gln Gln Asp Leu Asp Val Ala Lys Thr Leu Gly Asp Gln 260 265 270 Thr Gly Glu Cys Arg Ala His Gly Asn Leu Gly Ser Ala Phe Phe 275 280 285 Ser Lys Gly Asn Tyr Arg Glu Ala Leu Thr Asn His Arg His Gln 290 295 300 Leu Val Leu Ala Met Lys Leu Lys Asp Arg Glu Ala Ala Ser Ser 305 310 315 Ala Leu Ser Ser Leu Gly His Val Tyr Thr Ala Ile Gly Asp Tyr 320 325 330 Pro Asn Ala Leu Ala Ser His Lys Gln Cys Val Leu Leu Ala Lys 335 340 345 Gln Ser Lys Asp Glu Leu Ser Glu Ala Arg Glu Leu Gly Asn Met 350 355 360 Gly Ala Val Tyr Ile Ala Met Gly Asp Phe Glu Asn Ala Val Gln 365 370 375 Cys His Glu Gln His Leu Lys Ile Ala Lys Asp Leu Gly Asn Lys 380 385 390 Arg Glu Glu Ala Arg Ala Tyr Ser Asn Leu Gly Ser Ala Tyr His 395 400 405 Tyr Arg Arg Asn Phe Asp Lys Ala Met Ser Tyr His Asn Tyr Val 410 415 420 Leu Glu Leu Ala Gln Glu Leu Met Glu Lys Ala Ile Glu Met Arg 425 430 435 Ala Tyr Ala Gly Leu Gly His Ala Ala Arg Cys Met Gln Asp Leu 440 445 450 Glu Arg Ala Lys Gln Tyr His Glu Gln Gln Leu Gly Ile Ala Glu 455 460 465 Asp Leu Lys Asp Arg Ala Ala Glu Gly Arg Ala Ser Ser Asn Leu 470 475 480 Gly Ile Ile His Gln Met Lys Gly Asp Tyr Asp Thr Ala Leu Lys 485 490 495 Leu His Lys Thr His Leu Cys Ile Ala Gln Glu Leu Ser Asp Tyr 500 505 510 Ala Ala Gln Gly Arg Ala Tyr Gly Asn Met Gly Asn Ala Tyr Asn 515 520 525 Ala Leu Gly Met Tyr Asp Gln Ala Val Lys Tyr His Arg Gln Glu 530 535 540 Leu Gln Ile Ser Met Glu Val Asn Asp Arg Ala Ser Gln Ala Ser 545 550 555 Thr His Gly Asn Leu Ala Val Ala Tyr Gln Ala Leu Gly Ala His 560 565 570 Asp Arg Ala Leu Gln His Tyr Gln Asn His Leu Asn Ile Ala Arg 575 580 585 Glu Leu Arg Asp Ile Gln Ser Glu Ala Arg Ala Leu Ser Asn Leu 590 595 600 Gly Asn Phe His Cys Ser Arg Gly Glu Tyr Val Gln Ala Ala Pro 605 610 615 Tyr Tyr Glu Gln Tyr Leu Arg Leu Ala Pro Asp Leu Gln Asp Met 620 625 630 Glu Gly Glu Gly Lys Val Cys His Asn Leu Gly Tyr Ala His Tyr 635 640 645 Cys Leu Gly Asn Tyr Gln Glu Ala Val Lys Tyr Tyr Glu Gln Asp 650 655 660 Leu Ala Leu Ala Lys Asp Leu His Asp Lys Leu Ser Gln Ala Lys 665 670 675 Ala Tyr Cys Asn Leu Gly Leu Ala Phe Lys Ala Leu Leu Asn Phe 680 685 690 Ser Lys Ala Glu Glu Cys Gln Lys Tyr Leu Leu Ser Leu Ala Gln 695 700 705 Ser Leu Asn Asn Ser Gln Ala Lys Phe Arg Ala Leu Gly Asn Leu 710 715 720 Gly Asp Ile Phe Ile Cys Lys Lys Asp Ile Asn Gly Ala Ile Lys 725 730 735 Phe Tyr Glu Gln Gln Leu Gly Leu Ala His Gln Val Lys Asp Arg 740 745 750 Arg Leu Glu Ala Ser Ala Tyr Ala Ala Leu Gly Thr Ala Tyr Arg 755 760 765 Met Ile Gln Lys Tyr Asp Lys Ala Leu Gly Tyr His Thr Gln Glu 770 775 780 Leu Glu Val Tyr Gln Glu Leu Ser Asp Leu Pro Gly Glu Cys Arg 785 790 795 Ala His Gly His Leu Ala Ala Val Tyr Met Ala Leu Gly Lys Tyr 800 805 810 Thr Met Ala Phe Lys Cys Tyr Glu Glu Gln Leu Asp Leu Gly Gln 815 820 825 Lys Leu Lys Asp Pro Ser Leu Glu Ala Gln Val Tyr Gly Asn Met 830 835 840 Gly Ile Thr Lys Met Asn Met Asn Val Met Glu Glu Ala Ile Gly 845 850 855 Tyr Phe Glu Gln Gln Leu Ala Met Leu Gln Gln Leu Ser Gly Asn 860 865 870 Glu Ser Val Leu Asp Arg Gly Arg Ala Tyr Gly Asn Leu Gly Asp 875 880 885 Cys Tyr Glu Ala Leu Gly Asp Tyr Glu Glu Ala Ile Lys Tyr Tyr 890 895 900 Glu Gln Tyr Leu Ser Val Ala Gln Ser Leu Asn Arg Met Gln Asp 905 910 915 Gln Ala Lys Ala Tyr Arg Gly Leu Gly Asn Gly His Arg Ala Met 920 925 930 Gly Ser Leu Gln Gln Ala Leu Val Cys Phe Glu Lys Arg Leu Val 935 940 945 Val Ala His Glu Leu Gly Glu Ala Phe Asn Lys Ala Gln Ala Tyr 950 955 960 Gly Glu Leu Gly Ser Leu His Ser Gln Leu Gly Asn Tyr Glu Gln 965 970 975 Ala Ile Ser Cys Leu Glu Arg Gln Leu Asn Ile Ala Arg Asp Met 980 985 990 Lys Asp Arg Ala Leu Glu Ser Asp Ala Ala Cys Gly Leu Gly Gly 995 1000 1005 Val Tyr Gln Gln Met Gly Glu Tyr Asp Thr Ala Leu Gln Tyr His 1010 1015 1020 Gln Leu Asp Leu Gln Ile Ala Glu Glu Thr Asn Asn Pro Thr Cys 1025 1030 1035 Gln Gly Arg Ala Tyr Gly Asn Leu Gly Leu Thr Tyr Glu Ser Leu 1040 1045 1050 Gly Thr Phe Glu Arg Ala Val Val Tyr Gln Glu Gln His Leu Ser 1055 1060 1065 Ile Ala Ala Gln Met Asn Asp Leu Ala Ala Lys Thr Val Ser Tyr 1070 1075 1080 Ser Ser Leu Gly Arg Thr His His Ala Leu Gln Asn Tyr Ser Gln 1085 1090 1095 Ala Val Met Tyr Leu Gln Glu Gly Leu Arg Leu Ala Glu Gln Leu 1100 1105 1110 Gly Arg Arg Glu Asp Glu Ala Lys Ile Arg His Gly Leu Gly Leu 1115 1120 1125 Ser Leu Trp Ala Ser Gly Asn Leu Glu Glu Ala Gln His Gln Leu 1130 1135 1140 Tyr Arg Ala Ser Ala Leu Phe Glu Thr Ile Arg His Glu Ala Gln 1145 1150 1155 Leu Ser Thr Asp Tyr Lys Leu Ser Leu Phe Asp Leu Gln Thr Ser 1160 1165 1170 Ser Tyr Gln Ala Leu Gln Arg Val Leu Val Ser Leu Gly His His 1175 1180 1185 Asp Glu Ala Leu Ala Val Ala Glu Arg Gly Arg Thr Arg Ala Phe 1190 1195 1200 Ala Asp Leu Leu Val Glu Arg Gln Thr Gly Gln Gln Asp Ser Asp 1205 1210 1215 Pro Tyr Ser Pro Val Thr Ile Asp Gln Ile Leu Glu Met Val Asn 1220 1225 1230 Gly Gln Arg Gly Leu Val Leu Tyr Tyr Ser Leu Ala Ala Gly Tyr 1235 1240 1245 Leu Tyr Ser Trp Leu Leu Ala Pro Gly Ala Gly Ile Val Lys Phe 1250 1255 1260 His Glu His Tyr Leu Gly Glu Asn Thr Val Glu Asn Ser Ser Asp 1265 1270 1275 Phe Gln Ala Ser Ser Ser Val Thr Leu Pro Thr Ala Thr Gly Ser 1280 1285 1290 Ala Leu Glu Gln His Ile Ala Ser Val Arg Glu Ala Leu Gly Val 1295 1300 1305 Glu Ser His Tyr Ser Arg Ala Cys Ala Ser Ser Glu Thr Glu Ser 1310 1315 1320 Glu Ala Gly Asp Ile Met Asp Gln Gln Phe Glu Glu Met Asn Asn 1325 1330 1335 Lys Leu Asn Ser Val Thr Asp Pro Thr Gly Phe Leu Arg Met Val 1340 1345 1350 Arg Arg Asn Asn Leu Phe Asn Arg Ser Cys Gln Ser Met Thr Ser 1355 1360 1365 Leu Phe Ser Asn Thr Val Ser Pro Thr Gln Asp Gly Thr Ser Ser 1370 1375 1380 Leu Pro Arg Arg Gln Ser Ser Phe Ala Lys Pro Pro Leu Arg Ala 1385 1390 1395 Leu Tyr Asp Leu Leu Ile Ala Pro Met Glu Gly Gly Leu Met His 1400 1405 1410 Ser Ser Gly Pro Val Gly Arg His Arg Gln Leu Ile Leu Val Leu 1415 1420 1425 Glu Gly Glu Leu Tyr Leu Ile Pro Phe Ala Leu Leu Lys Gly Ser 1430 1435 1440 Ser Ser Asn Glu Tyr Leu Tyr Glu Arg Phe Gly Leu Leu Ala Val 1445 1450 1455 Pro Ser Ile Arg Ser Leu Ser Val Gln Ser Lys Ser His Leu Arg 1460 1465 1470 Lys Asn Pro Pro Thr Tyr Ser Ser Ser Thr Ser Met Ala Ala Val 1475 1480 1485 Ile Gly Asn Pro Lys Leu Pro Ser Ala Val Met Asp Arg Trp Leu 1490 1495 1500 Trp Gly Pro Met Pro Ser Ala Glu Glu Glu Ala Tyr Met Val Ser 1505 1510 1515 Glu Leu Leu Gly Cys Gln Pro Leu Val Gly Ser Val Ala Thr Lys 1520 1525 1530 Glu Arg Val Met Ser Ala Leu Thr Gln Ala Glu Cys Val His Phe 1535 1540 1545 Ala Thr His Ile Ser Trp Lys Leu Ser Ala Leu Val Leu Thr Pro 1550 1555 1560 Ser Met Asp Gly Asn Pro Ala Ser Ser Lys Ser Ser Phe Gly His 1565 1570 1575 Pro Tyr Thr Ile Pro Glu Ser Leu Arg Val Gln Asp Asp Ala Ser 1580 1585 1590 Asp Gly Glu Ser Ile Ser Asp Cys Pro Pro Leu Gln Glu Leu Leu 1595 1600 1605 Leu Thr Ala Ala Asp Val Leu Asp Leu Gln Leu Pro Val Lys Leu 1610 1615 1620 Val Val Leu Gly Ser Ser Gln Glu Ser Asn Ser Lys Val Thr Ala 1625 1630 1635 Asp Gly Val Ile Ala Leu Thr Arg Ala Phe Leu Ala Ala Gly Ala 1640 1645 1650 Gln Cys Val Leu Val Ser Leu Trp Pro Val Pro Val Ala Ala Ser 1655 1660 1665 Lys Met Phe Ile His Ala Phe Tyr Ser Ser Leu Leu Asn Gly Leu 1670 1675 1680 Lys Ala Ser Ala Ala Leu Gly Glu Ala Met Lys Val Val Gln Ser 1685 1690 1695 Ser Lys Ala Phe Ser His Pro Ser Asn Trp Ala Gly Phe Met Leu 1700 1705 1710 Ile Gly Ser Asp Val Lys Leu Asn Ser Pro Ser Ser Leu Ile Gly 1715 1720 1725 Gln Ala Leu Thr Glu Ile Leu Gln His Pro Glu Arg Ala Arg Asp 1730 1735 1740 Ala Leu Arg Val Leu Leu His Leu Val Glu Lys Ser Leu Gln Arg 1745 1750 1755 Ile Gln Asn Gly Gln Arg Asn Ala Met Tyr Thr Ser Gln Gln Ser 1760 1765 1770 Val Glu Asn Lys Val Gly Gly Ile Pro Gly Trp Gln Ala Leu Leu 1775 1780 1785 Thr Ala Val Gly Phe Arg Leu Asp Pro Pro Thr Ser Gly Leu Pro 1790 1795 1800 Ala Ala Val Phe Phe Pro Thr Ser Asp Pro Gly Asp Arg Leu Gln 1805 1810 1815 Gln Cys Ser Ser Thr Leu Gln Ser Leu Leu Gly Leu Pro Asn Pro 1820 1825 1830 Ala Leu Gln Ala Leu Cys Lys Leu Ile Thr Ala Ser Glu Thr Gly 1835 1840 1845 Glu Gln Leu Ile Ser Arg Ala Val Lys Asn Met Val Gly Met Leu 1850 1855 1860 His Gln Val Leu Val Gln Leu Gln Ala Gly Glu Lys Glu Gln Asp 1865 1870 1875 Leu Ala Ser Ala Pro Ile Gln Val Ser Ile Ser Val Gln Leu Trp 1880 1885 1890 Arg Leu Pro Gly Cys His Glu Phe Leu Ala Ala Leu Gly Phe Asp 1895 1900 1905 Leu Cys Glu Val Gly Gln Glu Glu Val Ile Leu Lys Thr Gly Lys 1910 1915 1920 Gln Ala Asn Arg Arg Thr Val His Phe Ala Leu Gln Ser Leu Leu 1925 1930 1935 Ser Leu Phe Asp Ser Thr Glu Leu Pro Lys Arg Leu Ser Leu Asp 1940 1945 1950 Ser Ser Ser Ser Leu Glu Ser Leu Ala Ser Ala Gln Ser Val Ser 1955 1960 1965 Asn Ala Leu Pro Leu Gly Tyr Gln Gln Pro Pro Phe Ser Pro Thr 1970 1975 1980 Gly Ala Asp Ser Ile Ala Ser Asp Ala Ile Ser Val Tyr Ser Leu 1985 1990 1995 Ser Ser Ile Ala Ser Ser Met Ser Phe Val Ser Lys Pro Glu Gly 2000 2005 2010 Gly Ser Glu Gly Gly Gly Pro Gly Gly Arg Gln Asp His Asp Arg 2015 2020 2025 Ser Lys Asn Ala Tyr Leu Gln Arg Ser Thr Leu Pro Arg Ser Gln 2030 2035 2040 Leu Pro Pro Gln Thr Arg Pro Ala Gly Asn Lys Asp Glu Glu Glu 2045 2050 2055 Tyr Glu Gly Phe Ser Ile Ile Ser Asn Glu Pro Leu Ala Thr Tyr 2060 2065 2070 Gln Glu Asn Arg Asn Thr Cys Phe Ser Pro Asp His Lys Gln Pro 2075 2080 2085 Gln Pro Gly Thr Ala Gly Gly Met Arg Val Ser Val Ser Ser Lys 2090 2095 2100 Gly Ser Ile Ser Thr Pro Asn Ser Pro Val Lys Met Thr Leu Ile 2105 2110 2115 Pro Ser Pro Asn Ser Pro Phe Gln Lys Val Gly Lys Leu Ala Ser 2120 2125 2130 Ser Asp Thr Gly Glu Ser Asp Gln Ser Ser Thr Glu Thr Asp Ser 2135 2140 2145 Thr Val Lys Ser Gln Glu Glu Ser Asn Pro Lys Leu Asp Pro Gln 2150 2155 2160 Glu Leu Ala Gln Lys Ile Leu Glu Glu Thr Gln Ser His Leu Ile 2165 2170 2175 Ala Val Glu Arg Leu Gln Arg Ser Gly Gly Gln Val Ser Lys Ser 2180 2185 2190 Asn Asn Pro Glu Asp Gly Val Gln Ala Pro Ser Ser Thr Ala Val 2195 2200 2205 Phe Arg Ala Ser Glu Thr Ser Ala Phe Ser Arg Pro Val Leu Ser 2210 2215 2220 His Gln Lys Ser Gln Pro Ser Pro Val Thr Val Lys Pro Lys Pro 2225 2230 2235 Pro Ala Arg Ser Ser Ser Leu Pro Lys Val Ser Ser Gly Tyr Ser 2240 2245 2250 Ser Pro Thr Thr Ser Glu Met Ser Ile Lys Asp Ser Pro Ser Gln 2255 2260 2265 His Ser Gly Arg Pro Ser Pro Gly Cys Asp Ser Gln Thr Ser Gln 2270 2275 2280 Leu Asp Gln Pro Leu Phe Lys Leu Lys Tyr Pro Ser Ser Pro Tyr 2285 2290 2295 Ser Ala His Ile Ser Lys Ser Pro Arg Asn Met Ser Pro Ser Ser 2300 2305 2310 Gly His Gln Ser Pro Ala Gly Ser Ala Pro Ser Pro Ala Leu Ser 2315 2320 2325 Tyr Ser Ser Ala Gly Ser Ala Arg Ser Ser Pro Ala Asp Ala Pro 2330 2335 2340 Asp Ile Asp Lys Leu Lys Met Ala Ala Ile Asp Glu Lys Val Gln 2345 2350 2355 Ala Val His Asn Leu Lys Met Phe Trp Gln Ser Thr Pro Gln His 2360 2365 2370 Ser Thr Gly Pro Met Lys Ile Phe Arg Gly Ala Pro Gly Thr Met 2375 2380 2385 Thr Ser Lys Arg Asp Val Leu Ser Leu Leu Asn Leu Ser Pro Arg 2390 2395 2400 His Asn Lys Lys Glu Glu Gly Val Asp Lys Leu Glu Leu Lys Glu 2405 2410 2415 Leu Ser Leu Gln Gln His Asp Gly Ala Pro Pro Lys Ala Pro Pro 2420 2425 2430 Asn Gly His Trp Arg Thr Glu Thr Thr Ser Leu Gly Ser Leu Pro 2435 2440 2445 Leu Pro Ala Gly Pro Pro Ala Thr Ala Pro Ala Arg Pro Leu Arg 2450 2455 2460 Leu Pro Ser Gly Asn Gly Tyr Lys Phe Leu Ser Pro Gly Arg Phe 2465 2470 2475 Phe Pro Ser Ser Lys Cys 2480 <210> SEQ ID NO 24 <211> LENGTH: 78 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1538253CD1 <400> SEQUENCE: 24 Met Ala His Cys Ser Leu Asp Leu Ser Gly Leu Ser Asp Pro Pro 1 5 10 15 Ala Ser Ala Ser Gln Ala Pro Gly Ser Thr Gly Val Gln His His 20 25 30 Val Gln Leu Ile Phe Lys Ile Phe Val Glu Met Glu Ser His Phe 35 40 45 Val Val Gln Ala Val Leu Thr Leu Leu Gly Leu Ser Asn Ser Ser 50 55 60 Ala Leu Ala Ser Gln Ser Val Gly Ile Thr Gly Glu Ser His Cys 65 70 75 Thr Arg Pro <210> SEQ ID NO 25 <211> LENGTH: 299 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 030658CD1 <400> SEQUENCE: 25 Met Met Leu Ile Pro Thr His His Phe Arg Asn Ile Glu Arg Lys 1 5 10 15 Pro Glu Tyr Leu Gln Pro Glu Lys Cys Val Pro Pro Pro Tyr Pro 20 25 30 Gly Pro Val Gly Thr Met Trp Phe Ile Arg Asp Gly Cys Gly Ile 35 40 45 Ala Cys Ala Ile Val Thr Trp Phe Leu Val Leu Tyr Ala Glu Phe 50 55 60 Val Val Leu Phe Val Met Leu Ile Pro Ser Arg Asp Tyr Val Tyr 65 70 75 Ser Ile Ile Asn Gly Ile Val Phe Asn Leu Leu Ala Phe Leu Ala 80 85 90 Leu Ala Ser His Cys Arg Ala Met Leu Thr Asp Pro Gly Ala Val 95 100 105 Pro Lys Gly Asn Ala Thr Lys Glu Phe Ile Glu Ser Leu Gln Leu 110 115 120 Lys Pro Gly Gln Val Val Tyr Lys Cys Pro Lys Cys Cys Ser Ile 125 130 135 Lys Pro Asp Arg Ala His His Cys Ser Val Cys Lys Arg Cys Ile 140 145 150 Arg Lys Met Asp His His Cys Pro Trp Val Asn Asn Cys Val Gly 155 160 165 Glu Asn Asn Gln Lys Tyr Phe Val Leu Phe Thr Met Tyr Ile Ala 170 175 180 Leu Ile Ser Leu His Ala Leu Ile Met Val Gly Phe His Phe Leu 185 190 195 His Cys Phe Glu Glu Asp Trp Thr Lys Cys Ser Ser Phe Ser Pro 200 205 210 Pro Thr Thr Val Ile Leu Leu Ile Leu Leu Cys Phe Glu Gly Leu 215 220 225 Leu Phe Leu Ile Phe Thr Ser Val Met Phe Gly Thr Gln Val His 230 235 240 Ser Ile Cys Thr Asp Glu Thr Gly Ile Glu Gln Leu Lys Lys Glu 245 250 255 Glu Arg Arg Trp Ala Lys Lys Thr Lys Trp Met Asn Met Lys Ala 260 265 270 Val Phe Gly His Pro Phe Ser Leu Gly Trp Ala Ser Pro Phe Ala 275 280 285 Thr Pro Asp Gln Gly Lys Ala Asp Pro Tyr Gln Tyr Val Val 290 295 <210> SEQ ID NO 26 <211> LENGTH: 243 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7486348CD1 <400> SEQUENCE: 26 Met Ala Cys Trp Trp Pro Leu Leu Leu Glu Leu Trp Thr Val Met 1 5 10 15 Pro Thr Trp Ala Gly Asp Glu Leu Leu Asn Ile Cys Met Asn Ala 20 25 30 Lys His His Lys Arg Val Pro Ser Pro Glu Asp Lys Leu Tyr Glu 35 40 45 Glu Cys Ile Pro Trp Lys Asp Asn Ala Cys Cys Thr Leu Thr Thr 50 55 60 Ser Trp Glu Ala His Leu Asp Val Ser Pro Leu Tyr Asn Phe Ser 65 70 75 Leu Phe His Cys Gly Leu Leu Met Pro Gly Cys Arg Lys His Phe 80 85 90 Ile Gln Ala Ile Cys Phe Tyr Glu Cys Ser Pro Asn Leu Gly Pro 95 100 105 Trp Ile Gln Pro Val Ala Pro Ser Gly Gln Gly Glu Arg Val Val 110 115 120 Asn Val Pro Leu Cys Gln Glu Asp Cys Glu Glu Trp Trp Glu Asp 125 130 135 Cys Arg Met Ser Tyr Thr Cys Lys Ser Asn Trp Arg Gly Gly Trp 140 145 150 Asp Trp Ser Gln Gly Lys Asn Arg Cys Pro Lys Gly Ala Gln Cys 155 160 165 Leu Pro Phe Ser His Tyr Phe Pro Thr Pro Ala Asp Leu Cys Glu 170 175 180 Lys Thr Trp Ser Asn Ser Phe Lys Ala Ser Pro Glu Arg Arg Asn 185 190 195 Ser Gly Arg Cys Leu Gln Lys Trp Phe Glu Pro Ala Gln Gly Asn 200 205 210 Pro Asn Val Ala Val Ala Arg Leu Phe Ala Ser Ser Ala Pro Ser 215 220 225 Trp Glu Leu Ser Tyr Thr Ile Met Val Cys Ser Leu Phe Leu Pro 230 235 240 Phe Leu Ser <210> SEQ ID NO 27 <211> LENGTH: 117 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3359663CD1 <400> SEQUENCE: 27 Met Ser Ala Pro Ala Gln Pro Pro Ala Glu Gly Thr Glu Gly Thr 1 5 10 15 Ala Pro Gly Gly Gly Pro Pro Gly Pro Pro Pro Asn Met Thr Ser 20 25 30 Asn Arg Arg Leu Gln Gln Thr Gln Ala Gln Val Glu Glu Val Val 35 40 45 Asp Ile Ile Arg Val Asn Val Asp Lys Val Leu Glu Arg Asp Gln 50 55 60 Lys Leu Ser Glu Leu Asp Asp Arg Ala Asp Ala Leu Gln Ala Gly 65 70 75 Ala Ser Gln Phe Glu Ser Ser Ala Ala Lys Leu Lys Arg Lys Tyr 80 85 90 Trp Trp Lys Asn Cys Lys Met Met Ile Met Leu Gly Ala Ile Phe 95 100 105 Ala Ile Ile Val Val Val Ile Val Ser Lys Tyr Arg 110 115 <210> SEQ ID NO 28 <211> LENGTH: 275 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3237418CD1 <400> SEQUENCE: 28 Met Ala Asn Phe Lys Gly His Ala Leu Pro Gly Ser Phe Phe Leu 1 5 10 15 Ile Ile Gly Leu Cys Trp Ser Val Lys Tyr Pro Leu Lys Tyr Phe 20 25 30 Ser His Thr Arg Lys Asn Ser Pro Leu His Tyr Tyr Gln Arg Leu 35 40 45 Glu Ile Val Glu Ala Ala Ile Arg Thr Leu Phe Ser Val Thr Gly 50 55 60 Ile Leu Ala Glu Gln Phe Val Pro Asp Gly Pro His Leu His Leu 65 70 75 Tyr His Glu Asn His Trp Ile Lys Leu Met Asn Trp Gln His Ser 80 85 90 Thr Met Tyr Leu Phe Phe Ala Val Ser Gly Ile Val Asp Met Leu 95 100 105 Thr Tyr Leu Val Ser His Val Pro Leu Gly Val Asp Arg Leu Val 110 115 120 Met Ala Val Ala Val Phe Met Glu Gly Phe Leu Phe Tyr Tyr His 125 130 135 Val His Asn Arg Pro Pro Leu Asp Gln His Ile His Ser Leu Leu 140 145 150 Leu Tyr Ala Leu Phe Gly Gly Cys Val Ser Ile Ser Leu Glu Val 155 160 165 Ile Phe Arg Asp His Ile Val Leu Glu Leu Phe Arg Thr Ser Leu 170 175 180 Ile Ile Leu Gln Gly Thr Trp Phe Trp Gln Ile Gly Phe Val Leu 185 190 195 Phe Pro Pro Phe Gly Thr Pro Glu Trp Asp Gln Lys Asp Asp Ala 200 205 210 Asn Leu Met Phe Ile Thr Met Cys Phe Cys Trp His Tyr Leu Ala 215 220 225 Ala Leu Ser Ile Val Ala Val Asn Tyr Ser Leu Val Tyr Cys Leu 230 235 240 Leu Thr Arg Met Lys Arg His Gly Arg Gly Glu Ile Ile Gly Ile 245 250 255 Gln Lys Leu Asn Ser Asp Asp Thr Tyr Gln Thr Ala Leu Leu Ser 260 265 270 Gly Ser Asp Glu Glu 275 <210> SEQ ID NO 29 <211> LENGTH: 268 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2529616CD1 <400> SEQUENCE: 29 Met Asn Ser Glu Lys Lys Gly Ile Arg Val Asn Phe Arg Arg Leu 1 5 10 15 Lys Lys Phe Asp Cys Lys Glu Lys Gln Met Leu Val Asp Lys Ala 20 25 30 Arg Glu Asp Tyr Ser Glu Ser Ile Asp Trp Cys Ile Ser Leu Ile 35 40 45 Cys Asp Tyr Arg Val Arg Ile Gly Cys Gly Ser Phe Thr Gly Ser 50 55 60 Leu Leu Glu Tyr Tyr Ala Ala Asp Ile Ser Tyr Pro Val Arg Lys 65 70 75 Glu Thr Lys Gln Asp Thr Phe Arg Asn Lys Phe Pro Lys Leu His 80 85 90 Asn Glu Asp Ala Arg Glu Pro Met Ala Val Thr Ser Gln Thr Lys 95 100 105 Lys Met Ser Phe Gln Lys Ile Leu Pro Asp Arg Met Lys Ala Ala 110 115 120 Arg Asp Arg Ala Asn Lys Asn Leu Val Asp Phe Ile Val Asn Ala 125 130 135 Lys Gly Thr Glu Asn His Leu Leu Ala Ile Val Asn Gly Thr Lys 140 145 150 Gly Ser Arg Trp Leu Lys Ser Phe Leu Asn Ala Asn Arg Phe Thr 155 160 165 Pro Cys Ile Glu Thr Tyr Phe Glu Asp Glu Asp Gln Leu Asp Glu 170 175 180 Val Val Lys Tyr Leu Gln Glu Val Cys Asn Gln Ile Asp Gln Ile 185 190 195 Met Pro Thr Trp Ile Lys Asp Asp Lys Ile Lys Phe Ile Leu Glu 200 205 210 Val Leu Leu Pro Glu Ala Ile Ile Cys Ser Ile Ser Ala Val Asp 215 220 225 Gly Leu Asp Tyr Glu Ala Ala Glu Ala Lys Tyr Leu Lys Gly Pro 230 235 240 Cys Leu Gly Tyr Arg Glu Arg Glu Leu Phe Asp Ala Lys Ile Ile 245 250 255 Tyr Glu Lys Arg Arg Lys Ala Pro Thr Asn Glu Ala His 260 265 <210> SEQ ID NO 30 <211> LENGTH: 848 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7475662CD1 <400> SEQUENCE: 30 Met Arg Thr Gln Ser Leu Leu Leu Leu Gly Ala Leu Leu Ala Val 1 5 10 15 Gly Ser Gln Leu Pro Ala Val Phe Gly Arg Lys Lys Gly Gly Ser 20 25 30 Thr Pro Gln Tyr Ser Ala Gln Leu Leu Arg Gly Lys Glu Leu Ala 35 40 45 Gln Gln Lys Pro Ser Leu Arg Arg Ala Thr Leu His Gly Gln Arg 50 55 60 Asn Ala Ser Glu Thr Glu Leu Thr Pro Asp Pro Arg Asn His Ala 65 70 75 Ile Cys Asn Ser Asp Glu Arg Asn Gly Ala Glu Asp Val Ala Ser 80 85 90 Cys Gly Cys Asp Ser Ala Pro Gly Trp Pro Leu Leu Thr His Glu 95 100 105 Gly Gly Gly Lys Phe Pro Ala Leu Ser Ala Gly Pro Leu Val Ser 110 115 120 Ser Thr Arg Leu Arg Asp Trp Ala Val His Cys Gly Gly Thr Leu 125 130 135 Gly Asn Pro Trp Ser Ser Phe Pro Val Leu Leu Thr Leu Gln Tyr 140 145 150 Asp Asp Arg Ala Ser Ala Leu Cys His Glu Lys Ser Leu Pro Gly 155 160 165 Ala Thr Cys Leu Ala Gly Glu Thr Pro Gly Ala Ser Leu Lys Leu 170 175 180 Ser Gln Thr Ser Gln Ala Ser Asn Leu Pro Lys Arg Lys Lys Tyr 185 190 195 Leu Trp Lys Asn Gly Tyr Arg Ser Thr Glu Val His Gln Glu Glu 200 205 210 Lys Lys Pro Val Leu Gln Val Leu Pro Val Arg Ser His Ser Arg 215 220 225 Leu Trp Gln Pro Gln Glu Ser Pro Arg Tyr Gln Leu Ser Gly Gly 230 235 240 Lys Thr Tyr Gln Glu Pro Val Cys Thr Lys Ala Val Lys Asp Pro 245 250 255 Arg Gly Ala Val Gly Thr Asn Glu Ser His Lys Asn Gly Gly Gly 260 265 270 Gly Ser Asp Lys Glu Pro Gly Ser Ser Gly Leu Phe Met Ser Ser 275 280 285 Cys Thr Tyr Pro Gly Leu Pro Lys Lys Lys Lys Tyr Asp Ala Thr 290 295 300 Arg Phe His Arg Gln Gly Asn Lys Pro Arg Glu Gly Asp Glu Cys 305 310 315 Thr Gln Gly Gln Gln Leu Val Met Leu Met Leu Leu Val Arg Gly 320 325 330 Thr His Tyr Glu Asn Leu Arg Ser Lys Val Val Leu Pro Thr Pro 335 340 345 Leu Gly Gly Arg Ser Thr Glu Thr Phe Val Ser Glu Phe Pro Gly 350 355 360 Pro Asp Thr Gly Ile Arg Trp Arg Arg Ser Asp Glu Ala Leu Arg 365 370 375 Val Asn Val Gly Gly Val Arg Arg Gln Leu Ser Ala Arg Ala Leu 380 385 390 Ala Arg Phe Pro Gly Thr Arg Leu Gly Arg Leu Gln Ala Ala Ala 395 400 405 Ser Glu Glu Gln Ala Arg Arg Leu Cys Asp Asp Tyr Asp Glu Ala 410 415 420 Ala Arg Glu Phe Tyr Phe Asp Arg His Pro Gly Phe Phe Leu Ser 425 430 435 Val Leu His Phe Tyr Arg Thr Gly His Leu His Val Leu Asp Glu 440 445 450 Leu Cys Val Phe Ala Phe Gly Gln Glu Ala Asp Tyr Trp Gly Leu 455 460 465 Gly Glu Asn Ala Leu Ala Ala Cys Cys Arg Ala Arg Tyr Leu Glu 470 475 480 Arg Arg Leu Thr Gln Pro His Ala Trp Asp Glu Asp Ser Asp Thr 485 490 495 Pro Ser Ser Val Asp Pro Cys Pro Asp Glu Ile Ser Asp Val Gln 500 505 510 Arg Glu Leu Ala Arg Tyr Gly Ala Ala Arg Cys Gly Arg Leu Arg 515 520 525 Arg Arg Leu Trp Leu Thr Met Glu Asn Pro Gly Tyr Ser Leu Pro 530 535 540 Ser Lys Leu Phe Ser Cys Val Ser Ile Ser Val Val Leu Ala Ser 545 550 555 Ile Ala Ala Met Cys Ile His Ser Leu Pro Glu Tyr Gln Ala Arg 560 565 570 Glu Ala Ala Ala Ala Val Ala Ala Val Ala Ala Gly Arg Ser Pro 575 580 585 Glu Gly Val Arg Asp Asp Pro Val Leu Arg Arg Leu Glu Tyr Phe 590 595 600 Cys Ile Ala Trp Phe Ser Phe Glu Val Ser Ser Arg Leu Leu Leu 605 610 615 Ala Pro Ser Thr Arg Asn Phe Phe Cys His Pro Leu Asn Leu Ile 620 625 630 Asp Ile Val Ser Val Leu Pro Phe Tyr Leu Thr Leu Leu Ala Gly 635 640 645 Val Ala Leu Gly Asp Gln Gly Gly Lys Glu Phe Gly His Leu Gly 650 655 660 Lys Val Val Gln Val Phe Arg Leu Met Arg Ile Phe Arg Val Leu 665 670 675 Lys Leu Ala Arg His Ser Thr Gly Leu Arg Ser Leu Gly Ala Thr 680 685 690 Leu Lys His Ser Tyr Arg Glu Val Gly Ile Leu Leu Leu Tyr Leu 695 700 705 Ala Val Gly Val Ser Val Phe Ser Gly Val Ala Tyr Thr Ala Glu 710 715 720 Lys Glu Glu Asp Val Gly Phe Asn Thr Ile Pro Ala Cys Trp Trp 725 730 735 Trp Gly Thr Val Ser Met Thr Thr Val Gly Tyr Gly Asp Val Val 740 745 750 Pro Val Thr Val Ala Gly Lys Leu Ala Ala Ser Gly Cys Ile Leu 755 760 765 Gly Gly Ile Leu Val Val Ala Leu Pro Ile Thr Ile Ile Phe Asn 770 775 780 Lys Phe Ser His Phe Tyr Arg Arg Gln Lys Ala Leu Glu Ala Ala 785 790 795 Val Arg Asn Ser Asn His Gln Glu Phe Glu Asp Leu Leu Ser Ser 800 805 810 Ile Asp Gly Val Ser Glu Ala Ser Leu Glu Thr Ser Arg Glu Thr 815 820 825 Ser Gln Glu Gly Gln Ser Ala Asp Leu Glu Ser Gln Ala Pro Ser 830 835 840 Glu Pro Pro His Pro Gln Met Tyr 845 <210> SEQ ID NO 31 <211> LENGTH: 273 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3811024CD1 <400> SEQUENCE: 31 Met Arg Leu Leu Val Leu Leu Trp Gly Cys Leu Leu Leu Pro Gly 1 5 10 15 Tyr Glu Ala Leu Glu Gly Pro Glu Glu Ile Ser Gly Phe Glu Gly 20 25 30 Asp Thr Val Ser Leu Gln Cys Thr Tyr Arg Glu Glu Leu Arg Asp 35 40 45 His Arg Lys Tyr Trp Cys Arg Lys Gly Gly Ile Leu Phe Ser Arg 50 55 60 Cys Ser Gly Thr Ile Tyr Ala Glu Glu Glu Gly Gln Glu Thr Met 65 70 75 Lys Gly Arg Val Ser Ile Arg Asp Ser Arg Gln Glu Leu Ser Leu 80 85 90 Ile Val Thr Leu Trp Asn Leu Thr Leu Gln Asp Ala Gly Glu Tyr 95 100 105 Trp Cys Gly Val Glu Lys Arg Gly Pro Asp Glu Ser Leu Leu Ile 110 115 120 Ser Leu Phe Val Phe Pro Ala Ser Pro Gly Leu Tyr Pro Ala Ala 125 130 135 Thr Thr Ala Lys Gln Gly Lys Thr Gly Ala Glu Ala Pro Pro Leu 140 145 150 Pro Gly Thr Ser Gln Tyr Gly His Glu Arg Thr Ser Gln Tyr Thr 155 160 165 Gly Thr Ser Pro His Pro Ala Thr Ser Pro Pro Ala Gly Ser Ser 170 175 180 Arg Pro Pro Met Gln Leu Asp Ser Thr Ser Ala Glu Asp Thr Ser 185 190 195 Pro Ala Leu Ser Ser Gly Ser Ser Lys Pro Arg Val Ser Ile Pro 200 205 210 Met Val Arg Ile Leu Ala Pro Val Leu Val Leu Leu Ser Leu Leu 215 220 225 Ser Ala Ala Gly Leu Ile Ala Phe Cys Ser His Leu Leu Leu Trp 230 235 240 Arg Lys Glu Ala Gln Gln Ala Thr Glu Thr Gln Arg Asn Glu Lys 245 250 255 Phe Cys Leu Ser Arg Leu Asn Ser Leu Met Phe Ser Leu Ser Leu 260 265 270 Pro Trp Leu <210> SEQ ID NO 32 <211> LENGTH: 311 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1683407CD1 <400> SEQUENCE: 32 Met Ala Gly Pro Leu Trp Arg Thr Ala Ala Phe Val Gln Arg His 1 5 10 15 Arg Thr Gly Leu Leu Val Gly Ser Cys Ala Gly Leu Phe Gly Val 20 25 30 Pro Val Ser Tyr His Leu Phe Pro Asp Pro Val Val Gln Trp Leu 35 40 45 Tyr Gln Tyr Trp Pro Gln Gly Gln Pro Ala Pro Leu Pro Pro Gln 50 55 60 Leu Gln Ser Leu Phe Gln Glu Val Leu Gln Asp Ile Gly Val Pro 65 70 75 Ser Gly His Cys Tyr Lys Pro Phe Thr Thr Phe Thr Phe Gln Pro 80 85 90 Val Ser Ala Gly Phe Pro Arg Leu Pro Ala Gly Ala Val Val Gly 95 100 105 Ile Pro Ala Ser Phe Leu Gly Asp Leu Val Ile Asn Thr Asn His 110 115 120 Pro Val Val Ile His Gly His Thr Val Asp Trp Arg Ser Pro Ala 125 130 135 Gly Ala Arg Leu Arg Ala Ser Leu Thr Leu Ser Arg Glu Ala Gln 140 145 150 Lys Phe Ala Leu Ala Arg Glu Val Val Tyr Leu Glu Ser Ser Thr 155 160 165 Thr Ala Val His Ala Leu Leu Ala Pro Ala Cys Leu Ala Gly Thr 170 175 180 Trp Ala Leu Gly Val Gly Ala Lys Tyr Thr Leu Gly Leu His Ala 185 190 195 Gly Pro Met Asn Leu Arg Ala Ala Phe Ser Leu Val Ala Ala Val 200 205 210 Ala Gly Phe Val Ala Tyr Ala Phe Ser Gln Asp Ser Leu Thr His 215 220 225 Ala Val Glu Ser Trp Leu Asp Arg Arg Thr Ala Ser Leu Ser Ala 230 235 240 Ala Tyr Ala Cys Gly Gly Val Glu Phe Tyr Glu Lys Leu Leu Ser 245 250 255 Gly Asn Leu Ala Leu Arg Ser Leu Leu Gly Lys Glu Gly Glu Lys 260 265 270 Leu Tyr Thr Pro Ser Gly Asn Ile Val Pro Arg His Leu Phe Arg 275 280 285 Ile Lys His Leu Pro Tyr Thr Thr Arg Arg Asp Ser Val Leu Gln 290 295 300 Met Trp Arg Gly Met Leu Asn Pro Gly Arg Ser 305 310 <210> SEQ ID NO 33 <211> LENGTH: 169 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1319969CD1 <400> SEQUENCE: 33 Met Leu Leu Thr Leu Ser Gly Leu Leu Leu Phe Glu Lys Pro Met 1 5 10 15 Gly Ile Cys Phe Ile Val Val Ser Leu Asn Ser Tyr Leu Ala Glu 20 25 30 Ser Ile Ser Gln Gly Lys Tyr Cys Ser Val Met Val Ser Trp Thr 35 40 45 Leu Phe Ser Ile Cys Phe Ser Thr Ser Ile Asn Gly Leu Leu Pro 50 55 60 Ala Ile Met Thr Cys Met His Leu Leu Ser Ser Phe Ser Lys Gln 65 70 75 Asn Lys Leu Cys Gly Cys Ile Ser Arg Thr Leu Ser His Phe Gln 80 85 90 Asp Ser Ile Glu Leu Glu Thr His Ile Asp Thr Ser Thr Gln Leu 95 100 105 Tyr Val Tyr Thr Glu His Ile Tyr Ser Asp Ile Phe Arg Lys Lys 110 115 120 Lys Lys Lys Lys Ile Gly Trp Thr Ile Gln Ile Trp Lys Tyr Ser 125 130 135 Leu Phe Asn His Leu Glu Pro Ile Leu Leu Thr Val Tyr Ile Cys 140 145 150 Arg Arg Asp Phe Val Lys Lys Thr His Met Cys Val Tyr Thr Gln 155 160 165 Ala Ser Ser Ser <210> SEQ ID NO 34 <211> LENGTH: 271 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1645034CD1 <400> SEQUENCE: 34 Met Pro Ala Ser Gln Ser Arg Ala Arg Ala Arg Asp Arg Asn Asn 1 5 10 15 Val Leu Asn Arg Ala Glu Phe Leu Ser Leu Asn Gln Pro Pro Lys 20 25 30 Gly Gly Pro Glu Pro Arg Ser Ser Gly Arg Lys Ala Ser Gly Pro 35 40 45 Ser Ala Gln Pro Pro Pro Ala Gly Asp Gly Ala Arg Glu Arg Arg 50 55 60 Gln Ser Gln Gln Leu Pro Glu Glu Asp Cys Met Gln Leu Asn Pro 65 70 75 Ser Phe Lys Gly Ile Ala Phe Asn Ser Leu Leu Ala Ile Asp Ile 80 85 90 Cys Met Ser Lys Arg Leu Gly Val Cys Ala Gly Arg Ala Ala Ser 95 100 105 Trp Ala Ser Ala Arg Ser Met Val Lys Leu Ile Gly Ile Thr Gly 110 115 120 His Gly Ile Pro Trp Ile Gly Gly Thr Ile Leu Cys Leu Val Lys 125 130 135 Ser Ser Thr Leu Ala Gly Gln Glu Val Leu Met Asn Leu Leu Leu 140 145 150 Ala Leu Leu Leu Asp Ile Met Thr Val Ala Gly Val Gln Lys Leu 155 160 165 Ile Lys Arg Arg Gly Pro Tyr Glu Met Ser Pro Ser Leu Leu Asp 170 175 180 Tyr Leu Thr Met Asp Ile Tyr Ala Phe Pro Ala Gly His Ala Ser 185 190 195 Arg Ala Ala Met Val Ser Lys Phe Phe Leu Ser His Leu Val Leu 200 205 210 Ala Val Pro Leu Arg Val Leu Leu Val Leu Trp Ala Leu Cys Val 215 220 225 Gly Leu Ser Arg Val Met Ile Gly Arg His His Val Thr Asp Val 230 235 240 Leu Ser Gly Phe Val Ile Gly Tyr Leu Gln Phe Arg Leu Val Glu 245 250 255 Leu Val Trp Met Pro Ser Ser Thr Cys Gln Met Leu Ile Ser Ala 260 265 270 Trp <210> SEQ ID NO 35 <211> LENGTH: 388 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7949783CD1 <400> SEQUENCE: 35 Met Ser Arg Arg Pro Pro Thr Gly Ala Thr Ile Glu Asp Arg Ile 1 5 10 15 Leu Arg Ile Thr Gly Tyr Tyr Gly Tyr Tyr Pro Gly Tyr Ser Ser 20 25 30 Gln Lys Thr Asp Asp Gly Thr Gln Thr His Ser Glu Asn Ser Ser 35 40 45 Gln Glu Lys Gln Asn Gln Gly Ser Leu Pro Val Leu His Val His 50 55 60 Gly Ser Glu Gly His Leu Gly Thr Leu Asp His Leu Val Ser Ile 65 70 75 Ile Ile Leu Val Tyr Tyr Ser Gly His Leu Ala Thr Ala Gln Glu 80 85 90 Lys Gln Ser Pro Met Lys Lys Phe Arg Glu Cys Ser Arg Ile Phe 95 100 105 Gly Glu Asp Gly Leu Thr Leu Lys Leu Phe Leu Lys Arg Thr Ala 110 115 120 Pro Phe Ser Ile Leu Trp Thr Leu Thr Asn Tyr Leu Tyr Leu Leu 125 130 135 Ala Leu Lys Lys Leu Thr Ala Thr Asp Val Ser Ala Leu Phe Cys 140 145 150 Cys Asn Lys Ala Phe Val Phe Leu Leu Ser Trp Ile Val Leu Lys 155 160 165 Asp Arg Phe Met Gly Val Arg Ile Val Ala Ala Ile Met Ala Ile 170 175 180 Thr Gly Ile Val Met Met Ala Tyr Ala Asp Asn Phe His Ala Asp 185 190 195 Ser Ile Ile Gly Val Ala Phe Ala Val Gly Ser Ala Ser Thr Ser 200 205 210 Ala Leu Tyr Lys Val Leu Phe Lys Met Phe Leu Gly Ser Ala Asn 215 220 225 Phe Gly Glu Ala Ala His Phe Val Ser Thr Leu Gly Phe Phe Asn 230 235 240 Leu Ile Phe Ile Ser Phe Thr Pro Val Ile Leu Tyr Phe Thr Lys 245 250 255 Val Glu His Trp Ser Ser Phe Ala Ala Leu Pro Trp Gly Cys Leu 260 265 270 Cys Gly Met Ala Gly Leu Trp Leu Ala Phe Asn Ile Leu Val Asn 275 280 285 Val Gly Val Val Leu Thr Tyr Pro Ile Leu Ile Ser Ile Gly Thr 290 295 300 Val Leu Ser Val Pro Gly Asn Ala Ala Val Asp Leu Leu Lys Gln 305 310 315 Glu Val Ile Phe Asn Val Val Arg Leu Ala Ala Thr Ile Ile Ile 320 325 330 Cys Ile Gly Phe Leu Leu Met Leu Leu Pro Glu Glu Trp Asp Glu 335 340 345 Ile Thr Leu Arg Phe Ile Asn Ser Leu Lys Glu Lys Lys Ser Glu 350 355 360 Glu His Val Asp Asp Val Thr Asp Pro Ser Ile His Leu Arg Gly 365 370 375 Arg Gly Arg Ala Asn Gly Thr Val Ser Ile Pro Leu Ala 380 385 <210> SEQ ID NO 36 <211> LENGTH: 726 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1265361CD1 <400> SEQUENCE: 36 Met Ala Ala Pro Gly Gly Arg Gly Arg Ser Leu Ser Gly Leu Leu 1 5 10 15 Pro Ala Gln Thr Ser Leu Glu Tyr Ala Leu Leu Asp Ala Val Thr 20 25 30 Gln Gln Glu Lys Asp Ser Leu Val Tyr Gln Tyr Leu Gln Lys Val 35 40 45 Asp Gly Trp Glu Gln Asp Leu Ser Val Pro Glu Phe Pro Glu Gly 50 55 60 Leu Glu Trp Leu Asn Thr Glu Glu Pro Ile Ser Val Tyr Lys Asp 65 70 75 Leu Cys Gly Lys Ile Val Val Leu Asp Phe Phe Thr Tyr Cys Cys 80 85 90 Ile Asn Cys Ile His Leu Leu Pro Asp Leu His Ala Leu Glu His 95 100 105 Thr Tyr Ser Asp Lys Asp Gly Leu Leu Ile Ile Gly Val His Ser 110 115 120 Ala Lys Phe Pro Asn Glu Lys Val Leu Asp Asn Ile Lys Ser Ala 125 130 135 Val Leu Arg Tyr Asn Ile Thr His Pro Met Val Asn Asp Ala Asp 140 145 150 Ala Ser Leu Trp Gln Glu Leu Glu Val Ser Cys Trp Pro Thr Leu 155 160 165 Val Ile Leu Gly Pro Arg Gly Asn Met Leu Phe Ser Leu Ile Gly 170 175 180 Glu Gly His Lys Asp Lys Leu Phe Leu Tyr Thr Ser Ile Ala Leu 185 190 195 Lys Tyr Tyr Lys Asp Arg Gly Gln Ile Arg Asp Asn Lys Ile Gly 200 205 210 Ile Lys Leu Tyr Lys Asp Ser Leu Pro Pro Ser Pro Leu Leu Phe 215 220 225 Pro Gly Lys Val Thr Val Asp Gln Val Thr Asp Arg Leu Val Ile 230 235 240 Ala Asp Thr Gly His His Arg Ile Leu Val Val Trp Lys Asn Gly 245 250 255 Gln Ile Gln Tyr Ser Ile Gly Gly Pro Asn Pro Gly Arg Lys Asp 260 265 270 Gly Ile Phe Ser Glu Ser Thr Phe Asn Ser Pro Gln Gly Val Ala 275 280 285 Ile Met Asn Asn Ile Ile Tyr Val Ala Asp Thr Glu Asn His Leu 290 295 300 Ile Arg Lys Ile Asp Leu Glu Ala Glu Lys Val Ser Thr Val Ala 305 310 315 Gly Ile Gly Ile Gln Gly Thr Asp Lys Glu Gly Gly Ala Lys Gly 320 325 330 Glu Gln Gln Pro Ile Ser Ser Pro Trp Asp Val Val Phe Gly Thr 335 340 345 Ser Gly Ser Glu Val Gln Arg Gly Asp Ile Leu Trp Ile Ala Met 350 355 360 Ala Gly Thr His Gln Ile Trp Ala Leu Leu Leu Asp Ser Gly Lys 365 370 375 Leu Pro Lys Lys Asn Glu Leu Thr Lys Gly Thr Cys Leu Arg Phe 380 385 390 Ala Gly Ser Gly Asn Glu Glu Asn Arg Asn Asn Ala Tyr Pro His 395 400 405 Lys Ala Gly Phe Ala Gln Pro Ser Gly Leu Ser Leu Ala Ser Glu 410 415 420 Asp Pro Trp Ser Cys Leu Phe Val Ala Asp Ser Glu Ser Ser Thr 425 430 435 Val Arg Thr Val Ser Leu Lys Asp Gly Ala Val Lys His Leu Val 440 445 450 Gly Gly Glu Arg Asp Pro Met Asn Leu Phe Ala Phe Gly Asp Val 455 460 465 Asp Gly Val Gly Ile Asn Ala Lys Leu Gln His Pro Leu Gly Val 470 475 480 Thr Trp Asp Lys Lys Arg Asn Leu Leu Tyr Val Ala Asp Ser Tyr 485 490 495 Asn His Lys Ile Lys Val Val Asp Pro Lys Thr Lys Asn Cys Thr 500 505 510 Thr Leu Ala Gly Thr Gly Asp Thr Asn Asn Val Thr Ser Ser Ser 515 520 525 Phe Thr Glu Ser Thr Phe Asn Glu Pro Gly Gly Leu Cys Ile Gly 530 535 540 Glu Asn Gly Glu Leu Leu Tyr Val Ala Asp Thr Asn Asn His Gln 545 550 555 Ile Lys Val Met Asp Leu Glu Thr Lys Met Val Ser Val Leu Pro 560 565 570 Ile Phe Arg Ser Glu Asn Ala Val Val Asp Gly Pro Phe Leu Val 575 580 585 Glu Lys Gln Lys Thr Leu Pro Lys Leu Pro Lys Ser Ala Pro Ser 590 595 600 Ile Arg Leu Ser Pro Val Thr Ala Cys Ala Gly Gln Thr Leu Gln 605 610 615 Phe Lys Leu Arg Leu Asp Leu Pro Ser Gly Ser Lys Leu Thr Glu 620 625 630 Gly Val Ser Ser Cys Trp Phe Leu Thr Ala Glu Gly Asn Glu Trp 635 640 645 Leu Leu Gln Gly Gln Ile Ala Ala Gly Asp Ile Glu Asn Ile Ser 650 655 660 Ser Gln Pro Thr Ile Ser Leu Gln Ile Pro Asp Asp Cys Leu Ser 665 670 675 Leu Glu Ala Ile Val Ser Val Ser Val Phe Leu Tyr Tyr Cys Ser 680 685 690 Ala Asp Ser Ser Ala Cys Met Met Lys Ala Ile Leu Phe Ser Gln 695 700 705 Pro Leu Gln Ile Thr Asp Thr Gln Gln Gly Cys Ile Ala Pro Val 710 715 720 Glu Leu Arg Tyr Val Phe 725 <210> SEQ ID NO 37 <211> LENGTH: 1651 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2645814CD1 <400> SEQUENCE: 37 Met Asp Ser Lys Lys Arg Ser Ser Thr Glu Ala Glu Gly Ser Lys 1 5 10 15 Glu Arg Gly Leu Val His Ile Trp Gln Ala Gly Ser Phe Pro Ile 20 25 30 Thr Pro Glu Arg Leu Pro Gly Trp Gly Gly Lys Thr Val Leu Gln 35 40 45 Ala Ala Leu Gly Val Lys His Gly Val Leu Leu Thr Glu Asp Gly 50 55 60 Glu Val Tyr Ser Phe Gly Thr Leu Pro Trp Arg Ser Gly Pro Val 65 70 75 Glu Ile Cys Pro Ser Ser Pro Ile Leu Glu Asn Ala Leu Val Gly 80 85 90 Gln Tyr Val Ile Thr Val Ala Thr Gly Ser Phe His Ser Gly Ala 95 100 105 Val Thr Asp Asn Gly Val Ala Tyr Met Trp Gly Glu Asn Ser Ala 110 115 120 Gly Gln Cys Ala Val Ala Asn Gln Gln Tyr Val Pro Glu Pro Asn 125 130 135 Pro Val Ser Ile Ala Asp Ser Glu Ala Ser Pro Leu Leu Ala Val 140 145 150 Arg Ile Leu Gln Leu Ala Cys Gly Glu Glu His Thr Leu Ala Leu 155 160 165 Ser Ile Ser Arg Glu Ile Trp Ala Trp Gly Thr Gly Cys Gln Leu 170 175 180 Gly Leu Ile Thr Thr Ala Phe Pro Val Thr Lys Pro Gln Lys Val 185 190 195 Glu His Leu Ala Gly Arg Val Val Leu Gln Val Ala Cys Gly Ala 200 205 210 Phe His Ser Leu Ala Leu Val Gln Cys Leu Pro Ser Gln Asp Leu 215 220 225 Lys Pro Val Pro Glu Arg Cys Asn Gln Cys Ser Gln Leu Leu Ile 230 235 240 Thr Met Thr Asp Lys Glu Asp His Val Ile Ile Ser Asp Ser His 245 250 255 Cys Cys Pro Leu Gly Val Thr Leu Thr Glu Ser Gln Ala Glu Asn 260 265 270 His Ala Ser Thr Ala Leu Ser Pro Ser Thr Glu Thr Leu Asp Arg 275 280 285 Gln Glu Glu Val Phe Glu Asn Thr Leu Val Ala Asn Asp Gln Ser 290 295 300 Val Ala Thr Glu Leu Asn Ala Val Ser Ala Gln Ile Thr Ser Ser 305 310 315 Asp Ala Met Ser Ser Gln Gln Asn Val Met Gly Thr Thr Glu Ile 320 325 330 Ser Ser Ala Arg Asn Ile Pro Ser Tyr Pro Asp Thr Gln Ala Val 335 340 345 Asn Glu Tyr Leu Arg Lys Leu Ser Asp His Ser Val Arg Glu Asp 350 355 360 Ser Glu His Gly Glu Lys Pro Val Pro Ser Gln Pro Leu Leu Glu 365 370 375 Glu Ala Ile Pro Asn Leu His Ser Pro Pro Thr Thr Ser Thr Ser 380 385 390 Ala Leu Asn Ser Leu Val Val Ser Cys Ala Ser Ala Val Gly Val 395 400 405 Arg Val Ala Ala Thr Tyr Glu Ala Gly Ala Leu Ser Leu Lys Lys 410 415 420 Val Met Asn Phe Tyr Ser Thr Thr Pro Cys Glu Thr Gly Ala Gln 425 430 435 Ala Gly Ser Ser Ala Ile Gly Pro Glu Gly Leu Lys Asp Ser Arg 440 445 450 Glu Glu Gln Val Lys Gln Glu Ser Met Gln Gly Lys Lys Ser Ser 455 460 465 Ser Leu Val Asp Ile Arg Glu Glu Glu Thr Glu Gly Gly Ser Arg 470 475 480 Arg Leu Ser Leu Pro Gly Leu Leu Ser Gln Val Ser Pro Arg Leu 485 490 495 Leu Arg Lys Ala Ala Arg Val Lys Thr Arg Thr Val Val Leu Thr 500 505 510 Pro Thr Tyr Ser Gly Glu Ala Asp Ala Leu Leu Pro Ser Leu Arg 515 520 525 Thr Glu Val Trp Thr Trp Gly Lys Gly Lys Glu Gly Gln Leu Gly 530 535 540 His Gly Asp Val Leu Pro Arg Leu Gln Pro Leu Cys Val Lys Cys 545 550 555 Leu Asp Gly Lys Glu Val Ile His Leu Glu Ala Gly Gly Tyr His 560 565 570 Ser Leu Ala Leu Thr Ala Lys Ser Gln Val Tyr Ser Trp Gly Ser 575 580 585 Asn Thr Phe Gly Gln Leu Gly His Ser Asp Phe Pro Thr Thr Val 590 595 600 Pro Arg Leu Ala Lys Ile Ser Ser Glu Asn Gly Val Trp Ser Ile 605 610 615 Ala Ala Gly Arg Asp Tyr Ser Leu Phe Leu Val Asp Thr Glu Asp 620 625 630 Phe Gln Pro Gly Leu Tyr Tyr Ser Gly Arg Gln Asp Pro Thr Glu 635 640 645 Gly Asp Asn Leu Pro Glu Asn His Ser Gly Ser Lys Thr Pro Val 650 655 660 Leu Leu Ser Cys Ser Lys Leu Gly Tyr Ile Ser Arg Val Thr Ala 665 670 675 Gly Lys Asp Ser Tyr Leu Ala Leu Val Asp Lys Asn Ile Met Gly 680 685 690 Tyr Ile Ala Ser Leu His Glu Leu Ala Thr Thr Glu Arg Arg Phe 695 700 705 Tyr Ser Lys Leu Ser Asp Ile Lys Ser Gln Ile Leu Arg Pro Leu 710 715 720 Leu Ser Leu Glu Asn Leu Gly Thr Thr Thr Thr Val Gln Leu Leu 725 730 735 Gln Glu Val Ala Ser Arg Phe Ser Lys Leu Cys Tyr Leu Ile Gly 740 745 750 Gln His Gly Ala Ser Leu Ser Ser Phe Leu His Gly Val Lys Glu 755 760 765 Ala Arg Ser Leu Val Ile Leu Lys His Ser Ser Leu Phe Leu Asp 770 775 780 Ser Tyr Thr Glu Tyr Cys Thr Ser Ile Thr Asn Phe Leu Val Met 785 790 795 Gly Gly Phe Gln Leu Leu Ala Lys Pro Ala Ile Asp Phe Leu Asn 800 805 810 Lys Asn Gln Glu Leu Leu Gln Asp Leu Ser Glu Val Asn Asp Glu 815 820 825 Asn Thr Gln Leu Met Glu Ile Leu Asn Thr Leu Phe Phe Leu Pro 830 835 840 Ile Arg Arg Leu His Asn Tyr Ala Lys Val Leu Leu Lys Leu Ala 845 850 855 Thr Cys Phe Glu Val Ala Ser Pro Glu Tyr Gln Lys Leu Gln Asp 860 865 870 Ser Ser Ser Cys Tyr Glu Cys Leu Ala Leu His Leu Gly Arg Lys 875 880 885 Arg Lys Glu Ala Glu Tyr Thr Leu Gly Phe Trp Lys Thr Phe Pro 890 895 900 Gly Lys Met Thr Asp Ser Leu Arg Lys Pro Glu Arg Arg Leu Leu 905 910 915 Cys Glu Ser Ser Asn Arg Ala Leu Ser Leu Gln His Ala Gly Arg 920 925 930 Phe Ser Val Asn Trp Phe Ile Leu Phe Asn Asp Ala Leu Val His 935 940 945 Ala Gln Phe Ser Thr His His Val Phe Pro Leu Ala Thr Leu Trp 950 955 960 Ala Glu Pro Leu Ser Glu Glu Ala Gly Gly Val Asn Gly Leu Lys 965 970 975 Ile Thr Thr Pro Glu Glu Gln Phe Thr Leu Ile Ser Ser Thr Pro 980 985 990 Gln Glu Lys Thr Lys Trp Leu Arg Ala Ile Ser Gln Ala Val Asp 995 1000 1005 Gln Ala Leu Arg Gly Met Ser Asp Leu Pro Pro Tyr Gly Ser Gly 1010 1015 1020 Ser Ser Val Gln Arg Gln Glu Pro Pro Ile Ser Arg Ser Ala Lys 1025 1030 1035 Tyr Thr Phe Tyr Lys Asp Pro Arg Leu Lys Asp Ala Thr Tyr Asp 1040 1045 1050 Gly Arg Trp Leu Ser Gly Lys Pro His Gly Arg Gly Val Leu Lys 1055 1060 1065 Trp Pro Asp Gly Lys Met Tyr Ser Gly Met Phe Arg Asn Gly Leu 1070 1075 1080 Glu Asp Gly Tyr Gly Glu Tyr Arg Ile Pro Asn Lys Ala Met Asn 1085 1090 1095 Lys Glu Asp His Tyr Val Gly His Trp Lys Glu Gly Lys Met Cys 1100 1105 1110 Gly Gln Gly Val Tyr Ser Tyr Ala Ser Gly Glu Val Phe Glu Gly 1115 1120 1125 Cys Phe Gln Asp Asn Met Arg His Gly His Gly Leu Leu Arg Ser 1130 1135 1140 Gly Lys Leu Thr Ser Ser Ser Pro Ser Met Phe Ile Gly Gln Trp 1145 1150 1155 Val Met Asp Lys Lys Ala Gly Tyr Gly Val Phe Asp Asp Ile Thr 1160 1165 1170 Arg Gly Glu Lys Tyr Met Gly Met Trp Gln Asp Asp Val Cys Gln 1175 1180 1185 Gly Asn Gly Val Val Val Thr Gln Phe Gly Leu Tyr Tyr Glu Gly 1190 1195 1200 Asn Phe His Leu Asn Lys Met Met Gly Asn Gly Val Leu Leu Ser 1205 1210 1215 Glu Asp Asp Thr Ile Tyr Glu Gly Glu Phe Ser Asp Asp Trp Thr 1220 1225 1230 Leu Ser Gly Lys Gly Thr Leu Thr Met Pro Asn Gly Asp Tyr Ile 1235 1240 1245 Glu Gly Tyr Phe Ser Gly Glu Trp Gly Ser Gly Ile Lys Ile Thr 1250 1255 1260 Gly Thr Tyr Phe Lys Pro Ser Leu Tyr Glu Ser Asp Lys Asp Arg 1265 1270 1275 Pro Lys Val Phe Arg Lys Leu Gly Asn Leu Ala Val Pro Ala Asp 1280 1285 1290 Glu Lys Trp Lys Ala Val Phe Asp Glu Cys Trp Arg Gln Leu Gly 1295 1300 1305 Cys Glu Gly Pro Gly Gln Gly Glu Val Trp Lys Ala Trp Asp Asn 1310 1315 1320 Ile Ala Val Ala Leu Thr Thr Ser Arg Arg Gln His Arg Asp Ser 1325 1330 1335 Pro Glu Ile Leu Ser Arg Ser Gln Thr Gln Thr Leu Glu Ser Leu 1340 1345 1350 Glu Phe Ile Pro Gln His Val Gly Ala Phe Ser Val Glu Lys Tyr 1355 1360 1365 Asp Asp Ile Arg Lys Tyr Leu Ile Lys Ala Cys Asp Thr Pro Leu 1370 1375 1380 His Pro Leu Gly Arg Leu Val Glu Thr Leu Val Ala Val Tyr Arg 1385 1390 1395 Met Thr Tyr Val Gly Val Gly Ala Asn Arg Arg Leu Leu Gln Glu 1400 1405 1410 Ala Val Lys Glu Ile Lys Ser Tyr Leu Lys Arg Ile Phe Gln Leu 1415 1420 1425 Val Arg Phe Leu Phe Pro Glu Leu Pro Glu Glu Gly Ser Thr Ile 1430 1435 1440 Pro Leu Ser Ala Pro Leu Pro Thr Glu Arg Lys Ser Phe Cys Thr 1445 1450 1455 Gly Lys Ser Asp Ser Arg Ser Glu Ser Pro Glu Pro Gly Tyr Val 1460 1465 1470 Val Thr Ser Ser Gly Leu Leu Leu Pro Val Leu Leu Pro Arg Leu 1475 1480 1485 Tyr Pro Pro Leu Phe Met Leu Tyr Ala Leu Asp Asn Asp Arg Glu 1490 1495 1500 Glu Asp Ile Tyr Trp Glu Cys Val Leu Arg Leu Asn Lys Gln Pro 1505 1510 1515 Asp Ile Ala Leu Leu Gly Phe Leu Gly Val Gln Arg Lys Phe Trp 1520 1525 1530 Pro Ala Thr Leu Ser Ile Leu Gly Glu Ser Lys Lys Val Leu Pro 1535 1540 1545 Thr Thr Lys Asp Ala Cys Phe Ala Ser Ala Val Glu Cys Leu Gln 1550 1555 1560 Gln Ile Ser Thr Thr Phe Thr Pro Ser Asp Lys Leu Lys Val Ile 1565 1570 1575 Gln Gln Thr Phe Glu Glu Ile Ser Gln Ser Val Leu Ala Ser Leu 1580 1585 1590 His Glu Asp Phe Leu Trp Ser Met Asp Asp Leu Phe Pro Val Phe 1595 1600 1605 Leu Tyr Val Val Leu Arg Ala Arg Ile Arg Asn Leu Gly Ser Glu 1610 1615 1620 Val His Leu Ile Glu Asp Leu Met Asp Pro Tyr Leu Gln His Gly 1625 1630 1635 Glu Gln Gly Ile Met Phe Thr Thr Leu Lys Val Ser Ile Val Ile 1640 1645 1650 Ile <210> SEQ ID NO 38 <211> LENGTH: 1112 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 695481CD1 <400> SEQUENCE: 38 Met Arg Trp Ser Pro Asp Asn Ser Val Val Ile Val Thr Trp Glu 1 5 10 15 Tyr Gly Gly Leu Ser Leu Trp Ser Val Phe Gly Ala Gln Leu Ile 20 25 30 Cys Thr Leu Gly Gly Asp Phe Ala Tyr Arg Ser Asp Gly Thr Lys 35 40 45 Lys Asp Pro Leu Lys Ile Asn Ser Met Ser Trp Gly Ala Glu Gly 50 55 60 Tyr His Leu Trp Val Ile Ser Gly Phe Gly Ser Gln Asn Thr Glu 65 70 75 Ile Glu Ser Asp Leu Arg Ser Val Val Lys Gln Pro Ser Ile Leu 80 85 90 Leu Phe Gln Phe Ile Lys Ser Val Leu Thr Val Asn Pro Cys Met 95 100 105 Ser Asn Gln Glu Gln Val Leu Leu Gln Gly Glu Asp Arg Leu Tyr 110 115 120 Leu Asn Cys Gly Glu Ala Ser Gln Thr Gln Asn Pro Arg Ser Ser 125 130 135 Ser Thr His Ser Glu His Lys Pro Ser Arg Glu Lys Ser Pro Phe 140 145 150 Ala Asp Gly Gly Leu Glu Ser Gln Gly Leu Ser Thr Leu Leu Gly 155 160 165 His Arg His Trp His Val Val Gln Ile Ser Ser Thr Tyr Leu Glu 170 175 180 Ser Asn Trp Pro Ile Arg Phe Ser Ala Ile Asp Lys Leu Gly Gln 185 190 195 Asn Ile Ala Val Val Gly Lys Phe Gly Phe Ala His Tyr Ser Leu 200 205 210 Leu Thr Lys Lys Trp Lys Leu Phe Gly Asn Ile Thr Gln Glu Gln 215 220 225 Asn Met Ile Val Thr Gly Gly Leu Ala Trp Trp Asn Asp Phe Met 230 235 240 Val Leu Ala Cys Tyr Asn Ile Asn Asp Arg Gln Glu Glu Leu Arg 245 250 255 Val Tyr Leu Arg Thr Ser Asn Leu Asp Asn Ala Phe Ala His Val 260 265 270 Thr Lys Ala Gln Ala Glu Thr Leu Leu Leu Ser Val Phe Gln Asp 275 280 285 Met Val Ile Val Phe Arg Ala Asp Cys Ser Ile Cys Leu Tyr Ser 290 295 300 Ile Glu Arg Lys Ser Asp Gly Pro Asn Thr Thr Ala Gly Ile Gln 305 310 315 Val Leu Gln Glu Val Ser Met Ser Arg Tyr Ile Pro His Pro Phe 320 325 330 Leu Val Val Ser Val Thr Leu Thr Ser Val Ser Thr Glu Asn Gly 335 340 345 Ile Thr Leu Lys Met Pro Gln Gln Ala Arg Gly Ala Glu Ser Ile 350 355 360 Met Leu Asn Leu Ala Gly Gln Leu Ile Met Met Gln Arg Asp Arg 365 370 375 Ser Gly Pro Gln Ile Arg Glu Lys Asp Ser Asn Pro Asn Asn Gln 380 385 390 Arg Lys Leu Leu Pro Phe Cys Pro Pro Val Val Leu Ala Gln Ser 395 400 405 Val Glu Asn Val Trp Thr Thr Cys Arg Ala Asn Lys Gln Lys Arg 410 415 420 His Leu Leu Glu Ala Leu Trp Leu Ser Cys Gly Gly Ala Gly Met 425 430 435 Lys Val Trp Leu Pro Leu Phe Pro Arg Asp His Arg Lys Pro His 440 445 450 Ser Phe Leu Ser Gln Arg Ile Met Leu Pro Phe His Ile Asn Ile 455 460 465 Tyr Pro Leu Ala Val Leu Phe Glu Asp Ala Leu Val Leu Gly Ala 470 475 480 Val Asn Asp Thr Leu Leu Tyr Asp Ser Leu Tyr Thr Arg Asn Asn 485 490 495 Ala Arg Glu Gln Leu Glu Val Leu Phe Pro Phe Cys Val Val Glu 500 505 510 Arg Thr Ser Gln Ile Tyr Leu His His Ile Leu Arg Gln Leu Leu 515 520 525 Val Arg Asn Leu Gly Glu Gln Ala Leu Leu Leu Ala Gln Ser Cys 530 535 540 Ala Thr Leu Pro Tyr Phe Pro His Val Leu Glu Leu Met Leu His 545 550 555 Glu Val Leu Glu Glu Glu Ala Thr Ser Arg Glu Pro Ile Pro Asp 560 565 570 Pro Leu Leu Pro Thr Val Ala Lys Phe Ile Thr Glu Phe Pro Leu 575 580 585 Phe Leu Gln Thr Val Val His Cys Ala Arg Lys Thr Glu Tyr Ala 590 595 600 Leu Trp Asn Tyr Leu Phe Ala Ala Val Gly Asn Pro Lys Asp Leu 605 610 615 Phe Glu Glu Cys Leu Met Ala Gln Asp Leu Asp Thr Ala Ala Ser 620 625 630 Tyr Leu Ile Ile Leu Gln Asn Met Glu Val Pro Ala Val Ser Arg 635 640 645 Gln His Ala Thr Leu Leu Phe Asn Thr Ala Leu Glu Gln Gly Lys 650 655 660 Trp Asp Leu Cys Arg His Met Ile Arg Phe Leu Lys Ala Ile Gly 665 670 675 Ser Gly Glu Ser Glu Thr Pro Pro Ser Thr Pro Thr Ala Gln Glu 680 685 690 Pro Ser Ser Ser Gly Gly Phe Glu Phe Phe Arg Asn Arg Ser Ile 695 700 705 Ser Leu Ser Gln Ser Ala Glu Asn Val Pro Ala Ser Lys Phe Ser 710 715 720 Leu Gln Lys Thr Leu Ser Met Pro Ser Gly Pro Ser Gly Lys Arg 725 730 735 Trp Ser Lys Asp Ser Asp Cys Ala Glu Asn Met Tyr Ile Asp Met 740 745 750 Met Leu Trp Arg His Ala Arg Arg Leu Leu Glu Asp Val Arg Leu 755 760 765 Lys Asp Leu Gly Cys Phe Ala Ala Gln Leu Gly Phe Glu Leu Ile 770 775 780 Ser Trp Leu Cys Lys Glu Arg Thr Arg Ala Ala Arg Val Asp Asn 785 790 795 Phe Val Ile Ala Leu Lys Arg Leu His Lys Asp Phe Leu Trp Pro 800 805 810 Leu Pro Ile Ile Pro Ala Ser Ser Ile Ser Ser Pro Phe Lys Asn 815 820 825 Gly Lys Tyr Arg Thr Val Gly Glu Gln Leu Leu Lys Ser Gln Ser 830 835 840 Ala Asp Pro Phe Leu Asn Leu Glu Met Asp Ala Gly Ile Ser Asn 845 850 855 Ile Gln Arg Ser Gln Ser Trp Leu Ser Asn Ile Gly Pro Thr His 860 865 870 His Glu Ile Asp Thr Ala Ser Ser His Gly Pro Gln Met Gln Asp 875 880 885 Ala Phe Leu Ser Pro Leu Ser Asn Lys Gly Asp Glu Cys Ser Ile 890 895 900 Gly Ser Ala Thr Asp Leu Thr Glu Ser Ser Ser Met Val Asp Gly 905 910 915 Asp Trp Thr Met Val Asp Glu Asn Phe Ser Thr Leu Ser Leu Thr 920 925 930 Gln Ser Glu Leu Glu His Ile Ser Met Glu Leu Ala Ser Lys Gly 935 940 945 Pro His Lys Ser Gln Val Gln Leu Arg Tyr Leu Leu His Ile Phe 950 955 960 Met Glu Ala Gly Cys Leu Asp Trp Cys Ile Val Ile Gly Leu Ile 965 970 975 Leu Arg Glu Ser Ser Ile Ile Asn Gln Ile Leu Val Ile Thr Gln 980 985 990 Ser Ser Glu Val Asp Gly Glu Met Leu Gln Asn Ile Lys Thr Gly 995 1000 1005 Leu His Ala Val Asp Arg Trp Ala Ser Thr Asp Cys Pro Gly Tyr 1010 1015 1020 Lys Pro Phe Leu Asn Ile Ile Lys Pro Gln Leu Gln Lys Leu Ser 1025 1030 1035 Glu Ile Thr Glu Glu Gln Val Gln Pro Asp Ala Phe Gln Pro Ile 1040 1045 1050 Thr Met Gly Lys Thr Pro Glu Gln Thr Ser Pro Arg Ala Glu Glu 1055 1060 1065 Ser Arg Gly Ser Ser Ser His Gly Ser Ile Pro Gln Gly Glu Val 1070 1075 1080 Gly Ser Ser Asn Met Val Ser Arg Lys Glu Glu Asp Thr Ala Gln 1085 1090 1095 Ala Glu Glu Glu Glu Pro Phe Gln Asp Gly Thr Tyr Asp Cys Ser 1100 1105 1110 Val Ser <210> SEQ ID NO 39 <211> LENGTH: 832 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 699941CD1 <400> SEQUENCE: 39 Met Leu Pro Phe Leu Leu Ala Thr Leu Gly Thr Thr Ala Leu Asn 1 5 10 15 Asn Ser Asn Pro Lys Asp Tyr Cys Tyr Ser Ala Arg Ile Arg Ser 20 25 30 Thr Val Leu Gln Gly Leu Pro Phe Gly Gly Val Pro Thr Val Leu 35 40 45 Ala Leu Asp Phe Met Cys Phe Leu Ala Leu Leu Phe Leu Phe Ser 50 55 60 Ile Leu Arg Lys Val Ala Trp Asp Tyr Gly Arg Leu Ala Leu Val 65 70 75 Thr Asp Ala Asp Arg Leu Arg Arg Gln Glu Arg Asp Arg Val Glu 80 85 90 Gln Glu Tyr Val Ala Ser Ala Met His Gly Asp Ser His Asp Arg 95 100 105 Tyr Glu Arg Leu Thr Ser Val Ser Ser Ser Val Asp Phe Asp Gln 110 115 120 Arg Asp Asn Gly Phe Cys Ser Trp Leu Thr Ala Ile Phe Arg Ile 125 130 135 Lys Asp Asp Glu Ile Arg Asp Lys Cys Gly Gly Asp Ala Val His 140 145 150 Tyr Leu Ser Phe Gln Arg His Ile Ile Gly Leu Leu Val Val Val 155 160 165 Gly Val Leu Ser Val Gly Ile Val Leu Pro Val Asn Phe Ser Gly 170 175 180 Asp Leu Leu Glu Asn Asn Ala Tyr Ser Phe Gly Arg Thr Thr Ile 185 190 195 Ala Asn Leu Lys Ser Gly Asn Asn Leu Leu Trp Leu His Thr Ser 200 205 210 Phe Ala Phe Leu Tyr Leu Leu Leu Thr Val Tyr Ser Met Arg Arg 215 220 225 His Thr Ser Lys Met Arg Tyr Lys Glu Asp Asp Leu Val Lys Arg 230 235 240 Thr Leu Phe Ile Asn Gly Ile Ser Lys Tyr Ala Glu Ser Glu Lys 245 250 255 Ile Lys Lys His Phe Glu Glu Ala Tyr Pro Asn Cys Thr Val Leu 260 265 270 Glu Ala Arg Pro Cys Tyr Asn Val Ala Arg Leu Met Phe Leu Asp 275 280 285 Ala Glu Arg Lys Lys Ala Glu Arg Gly Lys Leu Tyr Phe Thr Asn 290 295 300 Leu Gln Ser Lys Glu Asn Val Pro Thr Met Ile Asn Pro Lys Pro 305 310 315 Cys Gly His Leu Cys Cys Cys Val Val Arg Gly Cys Glu Gln Val 320 325 330 Glu Ala Ile Glu Tyr Tyr Thr Lys Leu Glu Gln Lys Leu Lys Glu 335 340 345 Asp Tyr Lys Arg Glu Lys Glu Lys Val Asn Glu Lys Pro Leu Gly 350 355 360 Met Ala Phe Val Thr Phe His Asn Glu Thr Ile Thr Ala Ile Ile 365 370 375 Leu Lys Asp Phe Asn Val Cys Lys Cys Gln Gly Cys Thr Cys Arg 380 385 390 Gly Glu Pro Arg Pro Ser Ser Cys Ser Glu Ser Leu His Ile Ser 395 400 405 Asn Trp Thr Val Ser Tyr Ala Pro Asp Pro Gln Asn Ile Tyr Trp 410 415 420 Glu His Leu Ser Ile Arg Gly Phe Ile Trp Trp Leu Arg Cys Leu 425 430 435 Val Ile Asn Val Val Leu Phe Ile Leu Leu Phe Phe Leu Thr Thr 440 445 450 Pro Ala Ile Ile Ile Thr Thr Met Asp Lys Phe Asn Val Thr Lys 455 460 465 Pro Val Glu Tyr Leu Asn Asn Pro Ile Ile Thr Gln Phe Phe Pro 470 475 480 Thr Leu Leu Leu Trp Cys Phe Ser Ala Leu Leu Pro Thr Ile Val 485 490 495 Tyr Tyr Ser Ala Phe Phe Glu Ala His Trp Thr Arg Ser Gly Glu 500 505 510 Asn Arg Thr Thr Met His Lys Cys Tyr Thr Phe Leu Ile Phe Met 515 520 525 Val Leu Leu Leu Pro Ser Leu Gly Leu Ser Ser Leu Asp Leu Phe 530 535 540 Phe Arg Trp Leu Phe Asp Lys Lys Phe Leu Ala Glu Ala Ala Ile 545 550 555 Arg Phe Glu Cys Val Phe Leu Pro Asp Asn Gly Ala Phe Phe Val 560 565 570 Asn Tyr Val Ile Ala Ser Ala Phe Ile Gly Asn Ala Met Asp Leu 575 580 585 Leu Arg Ile Pro Gly Leu Leu Met Tyr Met Ile Arg Leu Cys Leu 590 595 600 Ala Arg Ser Ala Ala Glu Arg Arg Asn Val Lys Arg His Gln Ala 605 610 615 Tyr Glu Phe Gln Phe Gly Ala Ala Tyr Ala Trp Met Met Cys Val 620 625 630 Phe Thr Val Val Met Thr Tyr Ser Ile Thr Cys Pro Ile Ile Val 635 640 645 Pro Phe Gly Leu Met Tyr Met Leu Leu Lys His Leu Val Asp Arg 650 655 660 Tyr Asn Leu Tyr Tyr Ala Tyr Leu Pro Ala Lys Leu Asp Lys Lys 665 670 675 Ile His Ser Gly Ala Val Asn Gln Val Val Ala Ala Pro Ile Leu 680 685 690 Cys Leu Phe Trp Leu Leu Phe Phe Ser Thr Met Arg Thr Gly Phe 695 700 705 Leu Ala Pro Thr Ser Met Phe Thr Phe Val Val Leu Val Ile Thr 710 715 720 Ile Val Ile Cys Leu Cys His Val Cys Phe Gly His Phe Lys Tyr 725 730 735 Leu Ser Ala His Asn Tyr Lys Ile Glu His Thr Glu Thr Asp Thr 740 745 750 Val Asp Pro Arg Ser Asn Gly Arg Pro Pro Thr Ala Ala Ala Val 755 760 765 Pro Lys Ser Ala Lys Tyr Ile Ala Gln Val Leu Gln Asp Ser Glu 770 775 780 Val Asp Gly Asp Gly Asp Gly Ala Pro Gly Ser Ser Gly Asp Glu 785 790 795 Pro Pro Ser Ser Ser Ser Gln Asp Glu Glu Leu Leu Met Pro Pro 800 805 810 Asp Ala Leu Thr Asp Thr Asp Phe Gln Ser Cys Glu Asp Ser Leu 815 820 825 Ile Glu Asn Glu Ile His Gln 830 <210> SEQ ID NO 40 <211> LENGTH: 807 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1515839CD1 <400> SEQUENCE: 40 Met Phe Ser Ala Gly Ala Glu Ser Leu Leu His Gln Ala Arg Glu 1 5 10 15 Ile Gln Asp Glu Glu Leu Lys Lys Phe Cys Ser Arg Ile Cys Lys 20 25 30 Leu Leu Gln Ala Glu Asp Leu Gly Pro Asp Thr Leu Asp Ser Leu 35 40 45 Gln Arg Leu Phe Leu Ile Ile Ser Ala Thr Lys Tyr Ser Arg Arg 50 55 60 Leu Glu Lys Thr Cys Val Asp Leu Leu Gln Ala Thr Leu Gly Leu 65 70 75 Pro Ala Cys Pro Glu Gln Leu Gln Val Leu Cys Ala Ala Ile Leu 80 85 90 Arg Glu Met Ser Pro Ser Asp Ser Leu Ser Leu Ala Trp Asp His 95 100 105 Thr Gln Asn Ser Arg Gln Leu Ser Leu Val Ala Ser Val Leu Leu 110 115 120 Ala Gln Gly Asp Arg Asn Glu Glu Val Arg Ala Val Gly Gln Gly 125 130 135 Val Leu Arg Ala Leu Glu Ser Arg Gln Pro Glu Gly Pro Ser Leu 140 145 150 Arg His Leu Leu Pro Val Met Ala Lys Val Val Val Leu Ser Pro 155 160 165 Gly Thr Leu Gln Glu Asp Gln Ala Thr Leu Leu Ser Lys Arg Leu 170 175 180 Val Asp Trp Leu Arg Tyr Ala Ser Leu Gln Gln Gly Leu Pro His 185 190 195 Ser Gly Gly Phe Phe Ser Thr Pro Arg Ala Arg Gln Pro Gly Pro 200 205 210 Val Thr Glu Val Asp Gly Ala Val Ala Thr Asp Phe Phe Thr Val 215 220 225 Leu Ser Ser Gly His Arg Phe Thr Asp Asp Gln Trp Leu Asn Val 230 235 240 Gln Ala Phe Ser Met Leu Arg Ala Trp Leu Leu His Ser Gly Pro 245 250 255 Glu Gly Pro Gly Thr Leu Asp Thr Asp Asp Arg Ser Glu Gln Glu 260 265 270 Gly Ser Thr Leu Ser Val Ile Ser Ala Thr Ser Ser Ala Gly Arg 275 280 285 Leu Leu Pro Pro Arg Glu Arg Leu Arg Glu Val Ala Phe Glu Tyr 290 295 300 Cys Gln Arg Leu Ile Glu Gln Ser Asn Arg Arg Ala Leu Arg Lys 305 310 315 Gly Asp Ser Asp Leu Gln Lys Ala Cys Leu Val Glu Ala Val Leu 320 325 330 Val Leu Asp Val Leu Cys Arg Gln Asp Pro Ser Phe Leu Tyr Arg 335 340 345 Ser Leu Ser Cys Leu Lys Ala Leu His Gly Arg Val Arg Gly Asp 350 355 360 Pro Ala Ser Val Arg Val Leu Leu Pro Leu Ala His Phe Phe Leu 365 370 375 Ser His Gly Glu Ala Ala Ala Val Asp Ser Glu Ala Val Tyr Gln 380 385 390 His Leu Phe Thr Arg Ile Pro Val Glu Gln Phe His Ser Pro Met 395 400 405 Leu Ala Phe Glu Phe Ile Gln Phe Cys Arg Asp Asn Leu His Leu 410 415 420 Phe Ser Gly His Leu Ser Thr Leu Arg Leu Ser Phe Pro Asn Leu 425 430 435 Phe Lys Phe Leu Ala Trp Asn Ser Pro Pro Leu Thr Ser Glu Phe 440 445 450 Val Ala Leu Leu Pro Ala Leu Val Asp Ala Gly Thr Ala Leu Glu 455 460 465 Met Leu His Ala Leu Leu Asp Leu Pro Cys Leu Thr Ala Val Leu 470 475 480 Asp Leu Gln Leu Arg Ser Ala Pro Ala Ala Ser Glu Arg Pro Leu 485 490 495 Trp Asp Thr Ser Leu Arg Ala Pro Ser Cys Leu Glu Ala Phe Arg 500 505 510 Asp Pro Gln Phe Gln Gly Leu Phe Gln Tyr Leu Leu Arg Pro Lys 515 520 525 Ala Ser Gly Ala Thr Glu Arg Leu Ala Pro Leu His Gln Leu Leu 530 535 540 Gln Pro Met Ala Gly Cys Ala Arg Val Ala Gln Cys Ala Gln Ala 545 550 555 Val Pro Thr Leu Leu Gln Ala Phe Phe Ser Ala Val Thr Gln Val 560 565 570 Ala Asp Gly Ser Leu Ile Asn Gln Leu Ala Leu Leu Leu Leu Gly 575 580 585 Arg Ser Asp Ser Leu Tyr Pro Ala Pro Gly Tyr Ala Ala Gly Val 590 595 600 His Ser Val Leu Ser Ser Gln Phe Leu Ala Leu Cys Thr Leu Lys 605 610 615 Pro Ser Leu Val Val Glu Leu Ala Arg Asp Leu Leu Glu Phe Leu 620 625 630 Gly Ser Val Asn Gly Leu Cys Ser Arg Ala Ser Leu Val Thr Ser 635 640 645 Val Val Trp Ala Ile Gly Glu Tyr Leu Ser Val Thr Tyr Asp Arg 650 655 660 Arg Cys Thr Val Glu Gln Ile Asn Lys Phe Phe Glu Ala Leu Glu 665 670 675 Ala Leu Leu Phe Glu Val Thr Gln Cys Arg Pro Ser Ala Ala Leu 680 685 690 Pro Arg Cys Pro Pro Gln Val Val Thr Val Leu Met Thr Thr Leu 695 700 705 Thr Lys Leu Ala Ser Arg Ser Gln Asp Leu Ile Pro Arg Ala Ser 710 715 720 Leu Leu Leu Ser Lys Met Arg Thr Leu Ala His Ser Pro Ala Thr 725 730 735 Ser Ser Thr His Ser Glu Glu Gly Ala Glu Ala Ile Arg Thr Arg 740 745 750 Ala Thr Glu Leu Leu Thr Leu Leu Lys Met Pro Ser Val Ala Gln 755 760 765 Phe Val Leu Thr Pro Ser Thr Glu Val Cys Ser Pro Arg Tyr His 770 775 780 Arg Asp Ala Asn Thr Ala Leu Pro Leu Ala Leu Arg Thr Val Ser 785 790 795 Arg Leu Val Glu Arg Glu Ala Gly Leu Met Pro Gly 800 805 <210> SEQ ID NO 41 <211> LENGTH: 511 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2300766CD1 <400> SEQUENCE: 41 Met Ala Asn Leu Pro Gly Tyr Ser Glu Glu Asp Lys Ser His Gly 1 5 10 15 Lys Asn Gln Val Ala Gly Tyr Gln Arg Lys Ser Trp Lys Tyr Ser 20 25 30 Ala Val Arg Arg Asp Gly Ser Phe His Tyr Val His Ser Thr Pro 35 40 45 Phe Gly Asn Tyr Ser Phe Ile Cys Val Asp Ala Thr Val Asn Pro 50 55 60 Gly Pro Lys Arg Pro Tyr Asn Phe Phe Gly Ile Leu Asp Lys Lys 65 70 75 Lys Met Glu Glu Leu Leu Leu Leu Ala Lys Glu Ser Ser Arg Ser 80 85 90 Asn His Thr Ile Trp Phe Gly His Phe Thr Thr Ser Thr Ile Leu 95 100 105 Ser Pro Ser Pro Gly Ile Arg Ser Ile Met Ser Ser Ala Ile Ala 110 115 120 Tyr Leu Cys Gly His Leu His Thr Leu Gly Gly Leu Met Pro Val 125 130 135 Leu His Thr Arg His Phe Gln Gly Thr Leu Glu Leu Glu Val Gly 140 145 150 Asp Trp Lys Asp Asn Arg Arg Tyr Arg Ile Phe Ala Phe Asp His 155 160 165 Asp Leu Phe Ser Phe Ala Asp Leu Ile Phe Gly Lys Trp Pro Val 170 175 180 Val Leu Ile Thr Asn Pro Lys Ser Leu Leu Tyr Ser Cys Gly Glu 185 190 195 His Glu Pro Leu Glu Arg Leu Leu His Ser Thr His Ile Arg Val 200 205 210 Leu Ala Phe Ser Leu Ser Ser Ile Thr Ser Val Thr Val Lys Ile 215 220 225 Asp Gly Val His Leu Gly Gln Ala Val His Val Ser Gly Pro Ile 230 235 240 Phe Val Leu Lys Trp Asn Pro Arg Asn Tyr Ser Ser Gly Thr His 245 250 255 Asn Ile Glu Val Ile Val Gln Asp Ser Ala Gly Arg Ser Lys Ser 260 265 270 Val His His Ile Phe Ser Val Gln Glu Asn Asn His Leu Ser Phe 275 280 285 Asp Pro Leu Ala Ser Phe Ile Leu Arg Thr Asp His Tyr Ile Met 290 295 300 Ala Arg Val Leu Phe Val Leu Ile Val Leu Ser Gln Leu Thr Ile 305 310 315 Leu Ile Ile Phe Arg Tyr Arg Gly Tyr Pro Glu Leu Lys Glu Pro 320 325 330 Ser Gly Phe Ile Asn Leu Thr Ser Phe Ser Leu His Val Leu Ser 335 340 345 Lys Ile Asn Ile Phe Tyr Tyr Ser Val Leu Leu Leu Thr Leu Tyr 350 355 360 Thr Val Leu Gly Pro Trp Phe Phe Gly Glu Ile Ile Asp Gly Lys 365 370 375 Phe Gly Cys Cys Phe Ser Phe Gly Ile Phe Val Asn Gly His Phe 380 385 390 Leu Gln Gly Ser Ile Thr Phe Ile Ile Gly Ile Leu Gln Leu Ala 395 400 405 Phe Phe Asn Ile Pro Leu Met Ala Tyr Met Cys Trp Ser Leu Leu 410 415 420 Gln Arg Cys Phe Gly His Asn Phe Arg Ser His Leu His Gln Arg 425 430 435 Lys Tyr Leu Lys Ile Met Pro Val His Leu Leu Met Leu Leu Leu 440 445 450 Tyr Ile Trp Gln Val Tyr Ser Cys Tyr Phe Leu Tyr Ala Thr Tyr 455 460 465 Gly Thr Leu Ala Phe Leu Phe Ser Pro Leu Arg Thr Trp Leu Thr 470 475 480 Leu Leu Thr Pro Val Leu Ile Arg Tyr Val Trp Thr Leu Asn Ser 485 490 495 Thr Lys Phe Gly Ile Phe Met Val Gln Leu Lys Ser His Leu Ser 500 505 510 Ser <210> SEQ ID NO 42 <211> LENGTH: 476 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7505816CD1 <400> SEQUENCE: 42 Met Ala Asn Leu Pro Gly Tyr Ser Glu Glu Asp Lys Ser His Gly 1 5 10 15 Lys Asn Gln Val Ala Gly Tyr Gln Arg Lys Ser Trp Lys Tyr Ser 20 25 30 Ala Val Arg Arg Asp Gly Ser Phe His Tyr Val His Ser Thr Pro 35 40 45 Phe Gly Asn Tyr Ser Phe Ile Cys Val Asp Ala Thr Val Asn Pro 50 55 60 Gly Pro Lys Arg Pro Tyr Asn Phe Phe Gly Ile Leu Asp Lys Lys 65 70 75 Lys Met Glu Glu Leu Leu Leu Leu Ala Lys Glu Ser Ser Arg Ser 80 85 90 Asn His Thr Ile Trp Phe Gly His Phe Thr Thr Ser Thr Ile Leu 95 100 105 Ser Pro Ser Pro Gly Ile Arg Ser Ile Met Ser Ser Ala Ile Ala 110 115 120 Tyr Leu Cys Gly His Leu His Thr Leu Gly Gly Leu Met Pro Val 125 130 135 Leu His Thr Arg His Phe Gln Gly Thr Leu Glu Leu Glu Val Gly 140 145 150 Asp Trp Lys Asp Asn Arg Arg Tyr Arg Ile Phe Ala Phe Asp His 155 160 165 Asp Leu Phe Ser Phe Ala Asp Leu Ile Phe Gly Lys Trp Pro Val 170 175 180 Val Leu Ile Thr Asn Pro Lys Ser Leu Leu Tyr Ser Cys Gly Glu 185 190 195 His Glu Pro Leu Glu Arg Leu Leu His Ser Thr His Ile Arg Val 200 205 210 Leu Ala Phe Ser Leu Ser Ser Ile Thr Ser Val Thr Val Lys Ile 215 220 225 Asp Gly Val His Leu Gly Gln Ala Val His Val Ser Gly Pro Ile 230 235 240 Phe Val Leu Lys Trp Asn Pro Arg Asn Tyr Ser Ser Gly Thr His 245 250 255 Asn Ile Glu Val Ile Val Gln Asp Ser Ala Gly Arg Ser Lys Ser 260 265 270 Val His His Ile Phe Ser Val Gln Glu Asn Asn His Leu Ser Phe 275 280 285 Asp Pro Leu Ala Ser Phe Ile Leu Arg Thr Asp His Tyr Ile Met 290 295 300 Ala Arg Val Leu Phe Val Leu Ile Val Leu Ser Gln Leu Thr Ile 305 310 315 Leu Ile Ile Phe Arg Tyr Arg Gly Tyr Pro Glu Leu Lys Gly Pro 320 325 330 Trp Phe Phe Gly Glu Ile Ile Asp Gly Lys Phe Gly Cys Cys Phe 335 340 345 Ser Phe Gly Ile Phe Val Asn Gly His Phe Leu Gln Gly Ser Ile 350 355 360 Thr Phe Ile Ile Gly Ile Leu Gln Leu Ala Phe Phe Asn Ile Pro 365 370 375 Leu Met Ala Tyr Met Cys Trp Ser Leu Leu Gln Arg Cys Phe Gly 380 385 390 His Asn Phe Arg Ser His Leu His Gln Arg Lys Tyr Leu Lys Ile 395 400 405 Met Pro Val His Leu Leu Met Leu Leu Leu Tyr Ile Trp Gln Val 410 415 420 Tyr Ser Cys Tyr Phe Leu Tyr Ala Thr Tyr Gly Thr Leu Ala Phe 425 430 435 Leu Phe Ser Pro Leu Arg Thr Trp Leu Thr Leu Leu Thr Pro Val 440 445 450 Leu Ile Arg Tyr Val Trp Thr Leu Asn Ser Thr Lys Phe Gly Ile 455 460 465 Phe Met Val Gln Leu Lys Ser His Leu Ser Ser 470 475 <210> SEQ ID NO 43 <211> LENGTH: 206 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7504118CD1 <400> SEQUENCE: 43 Met Ala Asn Phe Lys Gly His Ala Leu Pro Gly Ser Phe Phe Leu 1 5 10 15 Ile Ile Gly Leu Cys Trp Ser Val Lys Tyr Pro Leu Lys Tyr Phe 20 25 30 Ser His Thr Arg Lys Asn Ser Pro Leu His Tyr Tyr Gln Arg Leu 35 40 45 Glu Ile Val Glu Ala Ala Ile Arg Thr Leu Phe Ser Val Thr Gly 50 55 60 Phe Leu Phe Tyr Tyr His Val His Asn Arg Pro Pro Leu Asp Gln 65 70 75 His Ile His Ser Leu Leu Leu Tyr Ala Leu Phe Gly Gly Cys Val 80 85 90 Ser Ile Ser Leu Glu Val Ile Phe Arg Asp His Ile Val Leu Glu 95 100 105 Leu Phe Arg Thr Ser Leu Ile Ile Leu Gln Gly Thr Trp Phe Trp 110 115 120 Gln Ile Gly Phe Val Leu Phe Pro Pro Phe Gly Thr Pro Glu Trp 125 130 135 Asp Gln Lys Asp Asp Ala Asn Leu Met Phe Ile Thr Met Cys Phe 140 145 150 Cys Trp His Tyr Leu Ala Ala Leu Ser Ile Val Ala Val Asn Tyr 155 160 165 Ser Leu Val Tyr Cys Leu Leu Thr Arg Met Lys Arg His Gly Arg 170 175 180 Gly Glu Ile Ile Gly Ile Gln Lys Leu Asn Ser Asp Asp Thr Tyr 185 190 195 Gln Thr Ala Leu Leu Ser Gly Ser Asp Glu Glu 200 205 <210> SEQ ID NO 44 <211> LENGTH: 6625 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2489747CB1 <400> SEQUENCE: 44 gcgggaggtg acgcgcggcg aggatggcgg cgcggggccg ggggctgctg ctgctgacgc 60 tgtcggtgct gttggcggcg ggcccctccg ccgctgcggc caagctcaac atccccaaag 120 tgctgctgcc cttcacgcgg gccacgcgcg ttaacttcac gctggaggcc tcggagggct 180 gctaccgctg gttgtccacc cggccggagg tggccagcat cgagccgctg ggcctggacg 240 agcagcagtg ctcccagaag gcagtggtgc aggcccgcct gacccagcct gcccgcctca 300 ccagcatcat cttcgcagag gacatcacca caggccaggt cctgcgctgt gatgccattg 360 tggacctcat ccatgacatc cagatcgtct ccaccacccg cgagctctac ctggaggact 420 cccccctgga gctgaagatc caggccctgg actccgaagg gaacaccttc agcactctgg 480 ctggactggt cttcgagtgg acgattgtga aggactccga ggcggacagg ttctcagact 540 cccacaatgc gctgcgaatc ctcactttct tggagtctac gtacatccct ccttcttaca 600 tctcagagat ggagaaggct gccaagcaag gggacaccat cctggtgtct gggatgaaga 660 ccgggagctc caagctcaag gctcgcatcc aggaggctgt ctacaagaat gtacgccctg 720 cagaagtcag gctgctgatt ttggaaaaca tccttctgaa cccggcctat gacgtctacc 780 tgatggtggg aacctccatt cactacaagg tgcagaagat caggcaaggg aaaattacag 840 aactctccat gccttccgat cagtacgagt tgcagcttca gaacagcatc ccgggccccg 900 aaggagaccc aacccggccg gtggctgtct tggcccagga cacgtcgatg gtcactgcac 960 tgcagctggg acagagcagc ctcgtccttg gccacaggag tattcgcatg caaggtgctt 1020 ctaggttacc caacagcact atctacgtgg tcgaacctgg atacctaggg ttcactgttc 1080 accctggtga caggtgggtg ctggagaccg gccgcctgta tgaaatcacc atcgaagttt 1140 ttgacaagtt cagcaacaag gtctatgtat ctgacaacat ccgaattgaa actgtgcttc 1200 ctgctgagtt cttcgaggtg ctctcgtcct cccagaatgg gtcataccat cgcatcaggg 1260 cactaaagag gggacagacg gccattgacg cggccctcac ctctgtggtg gaccaggatg 1320 gaggggtcca catactacag gtgcctgtgt ggaaccagca ggaggtggaa attcacatcc 1380 cgatcaccct gtatcccagc atcttgacat ttccgtggca accaaagacg ggcgcctatc 1440 agtacacaat aagggcccac ggtggcagtg ggaacttcag ctggtcttcg tcaagccacc 1500 tggttgccac agttactgtc aagggcgtga tgaccacagg cagtgacatc gggttcagtg 1560 tgatccaggc acatgatgtg cagaacccac tccatttcgg tgagatgaag gtgtatgtga 1620 tcgagcccca cagcatggag tttgccccgt gccaggtgga ggcacgtgtg ggccaggccc 1680 tggagctgcc cctgaggatc agtggcctca tgcccggcgg ggccagtgag gtggtcacct 1740 tgagcgactg ctcccacttt gacttggctg tcgaggtgga gaaccagggt gtgttccagc 1800 cactcccagg gaggctgccg ccaggctctg agcactgcag cggcgtccgg gtaaaggccg 1860 aggcccaggg ctctaccacg cttcttgtga gctacagaca cggccacgtc cacctgagtg 1920 ccaagatcac cattgctgcc tacctgcccc tcaaggctgt ggatccctcc tctgttgcct 1980 tggtaaccct gggctcctca aaggagatgc tgtttgaagg aggtcccaga ccttggatcc 2040 tcgagccgtc caaattcttc cagaacgtca ccgctgagga cactgacagc atcggcctgg 2100 ctctctttgc cccccattcc tcccggaatt atcagcaaca ctggatcctt gtgacctgtc 2160 aggccttggg tgagcaggtc atcgccctgt cggtggggaa caagcccagc ctcaccaacc 2220 cctttcctgc ggtggagcct gccgtggtga agttcgtctg cgccccaccg tccaggctca 2280 ccctcgcgcc tgtctacacc agcccccagc tggacatgtc ctgtccgctg ctgcagcaga 2340 acaagcaggt ggtcccagtg tccagccacc gcaaccccct gctggacctg gctgcttacg 2400 accaggaggg ccgccggttc gacaacttca gctctctgag catccagtgg gagtccacca 2460 ggccagtgtt ggccagcatc gagcctgagc tgcccatgca gctggtgtcc caggacgatg 2520 agagtggcca aaagaagctg cacggtttgc aggccatttt ggttcacgag gcatcaggaa 2580 ccacagccat cactgccact gccactggct accaggagtc ccacctcagc tctgccagaa 2640 caaagcagcc gcatgaccct ctggtgcctc tgtcggcctc catagagctc atcctggtgg 2700 aggacgtgag ggtgagccca gaagaggtga ccatctacaa ccaccctggc atccaggcag 2760 agctccgcat cagggaaggc tcaggttact tcttcctcaa caccagcacc gcagatgttg 2820 tcaaggtggc ctaccaggag gccaggggtg tcgccatggt gcaccctttg ctcccgggct 2880 catccaccat catgatccat gacttgtgcc tcgtcttccc ggccccagcc aaggctgtcg 2940 tttacgtgtc ggacattcag gagctgtaca tccgtgtggt tgacaaggtg gagattggga 3000 agacagtgaa ggcatacgtc cgcgtgctgg acttgcacaa gaagcccttc cttgccaaat 3060 acttcccctt catggacctg aagctccgag cagcctcccc gatcattaca ttggtggccc 3120 ttgatgaagc ccttgacaac tacaccatca cattcctcat ccgcggtgtg gccatcggcc 3180 agaccagtct aactgcaagt gtgaccaata aagctggaca gagaatcaac tcagccccac 3240 aacagattga agtctttccc ccgttcaggc tgatgcccag gaaggtgaca ctgcttatcg 3300 gggccacgat gcaggtcacc tccgagggcg gcccccagcc tcagtccaac atccttttct 3360 ccatcagcaa tgagagcgtt gcgctggtga gcgctgctgg gctggtacag ggcctcgcca 3420 tcgggaacgg cactgtgtct gggctcgtgc aggcagtgga tgcagagacc ggcaaggtgg 3480 tcatcatctc tcaggacctc gtgcaggtgg aagtgctgct gctaagggcc gtgaggatcc 3540 gcgcccccat catgcggatg aggacgggca cccagatgcc catctatgtc accggcatca 3600 ccaaccacca gaaccctttc tcctttggca atgccgtgcc aggcctgacc ttccactggt 3660 ctgtcaccaa gcgggacgtc ctggacctcc gagggcggca ccacgaggcg tcgatccgac 3720 tcccgtcaca gtacaacttt gccatgaacg tgctcggccg ggtaaaaggc cggaccgggc 3780 tgagggtggt ggtcaaggct gtggacccca catcggggca gctgtatggc ctggccagag 3840 aactctcgga tgagatccaa gtccaggtgt ttgagaagct gcagctgctc aaccctgaaa 3900 tagaagcaga acaaatatta atgtcgccca actcatatat aaagctgcag acaaacaggg 3960 atggtgcagc ctctctgagc taccgcgtcc tggatggacc cgaaaaggtt ccagttgtgc 4020 atgttgatga gaaaggcttt ctagcatcag ggtctatgat cgggacatcc accatcgaag 4080 tgattgcaca agagcccttt ggggccaacc aaaccatcat tgttgctgta aaggtatccc 4140 ctgtttccta cctgagggtt tccatgagcc ctgtcctgca cacccagaac aaggaggccc 4200 tggtggccgt gcctttggga atgaccgtga ccttcactgt ccacttccac gacaactctg 4260 gagatgtctt ccatgctcac agttcggtcc tcaactttgc cactaacaga gacgactttg 4320 tgcagatcgg gaagggcccc accaacaaca cctgtgttgt ccgcacagtc agcgtgggcc 4380 tgacactgct ccgtgtgtgg gacgcagagc acccgggcct ctcggacttc atgcccctgc 4440 ctgtcctaca ggccatctcc ccagagctgt ctggggccat ggtggtgggg gacgtgctct 4500 gtctggccac tgttctgacc agcctggaag gcctctcagg aacctggagc tcctcggcca 4560 acagcatcct ccacatcgac cccaagacgg gtgtggctgt ggcccgggcc gtgggatccg 4620 tgacggttta ctatgaggtc gctgggcacc tgaggaccta caaggaggtg gtggtcagcg 4680 tccctcagag gatcatggcc cgtcacctcc accccatcca gaccagcttc caggaggcta 4740 cagcctccaa agtgattgtt gccgtgggag acagaagctc taacctgaga ggcgagtgca 4800 cccccaccca gagggaagtc atccaggcct tgcacccaga gaccctcatc agctgccagt 4860 cccagttcaa gccggccgtc tttgatttcc catctcaaga tgtgttcacc gtggagccac 4920 agtttgacac tgctctcggc cagtacttct gctcaatcac aatgcacagg ctgacggaca 4980 agcagcggaa gcacctgagc atgaagaaga cagctctggt ggtcagtgcc tccctctcca 5040 gcagccactt ctccacagag caggtggggg ccgaggtgcc cttcagccca ggtctcttcg 5100 ccgaccaggc tgaaatcctt ttgagcaacc actacaccag ttccgagatc agggtctttg 5160 gtgccccgga ggttctggag aacttggagg tgaaatccgg gtccccggcc gtgctggcat 5220 tcgcaaagga gaagtctttt gggtggccca gcttcatcac atacacggtc ggcgtcttgg 5280 accccgcggc tggcagccaa gggcctctgt ccactaccct gaccttctcc agccccgtga 5340 ccaaccaagc cattgccatc ccagtgacag tggcttttgt ggtggatcgc cgtgggcccg 5400 gtccttatgg agccagcctc ttccagcact tcctggattc ctaccaggtc atgttcttca 5460 cgctcttcgc cctgttggct gggacagcgg tcatgatcat agcctaccac actgtctgca 5520 cgccccggga tcttgctgtg cctgcagccc tcacgcctcg agccagccct ggacacagcc 5580 cccactattt cgctgcctca tcacccacat ctcccaatgc attgcctcct gctcgcaaag 5640 ccagccctcc ctcagggctg tggagcccag cctatgcctc ccactaggcc gcgtgaaggt 5700 tcccggagga tgggtctcag ccgagcctcg tgcaccccca agatggaaca tccctgctgc 5760 attcacactg gaacaagccc ctccagatga gtgccccggc cccaggccag cttcactgcc 5820 gtctcttcac acagagctgt agtttcggct ctgcccatta gctcatttta tgtaggagtt 5880 ttaaatgtgt gtttttttcc tttcaagtct tacaaagcta agactttttg gctcattcct 5940 ttttgcatgg ttgtctaggg tttctggaca atgtgctgtt gcatttttat tttcctagcc 6000 ttgctaaaat ctttcccttc tcaagacttt gagcagttag aagtgctctt tagaagttgt 6060 ctgtgggtga tgttactgta gtggtctcag ggaaaggatt gtccagttac tttagggggt 6120 ttttggtggg gtttttcccc ctgtgaaaac ttactttgcc cctagtctgg ctgctgctag 6180 gacttctgag gagcaatggg acatgagtgt ccctgtatct gcgccactgc cgcaagggaa 6240 gcctcaggaa ccagcacctg gaggccagga tagccaagcc ctgggtgagc gagaggctgg 6300 agaacacagg agctcaccca gggctgctgc ccaaccatgg gccactgtga acagacttca 6360 gtcctctgtt tttgtttcat aagccgttga gacatctgat ggacttggct taggccctgc 6420 tgggacatcc cacgtgtgat ccctttcact ccatcaggac accaggactg tccttaggaa 6480 aatgtccttg agatggcagc aggagtcata ttttctgtgt gtgtgtttcg gaaagccgct 6540 gtgtcctgcc tcagcacaaa gacccagtgt catttgctcc tcctgttcct gtgccactcc 6600 agaacctcag cagatctgag ccacc 6625 <210> SEQ ID NO 45 <211> LENGTH: 2962 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5857405CB1 <400> SEQUENCE: 45 gccccgcttg cccactcccc acttcccgag ccggctccgt gtttagggag ggcagtgatc 60 acgcaagccg gagcggcggg ctgacgttgg acgagctgcc aggtagctga aagcaggcag 120 ccaggcagcc gagacacttc ccagcgattc cagcctgggc tccgcaggaa gcctcgctga 180 atcccagcca gctggttcta accttccaga atcgcaatcc cttctcccca cagccagccc 240 tcgccgagca agcagcagga tgtttgcagt gtcgcgccca gggctctgag actgagcctg 300 ccatccactc gcacgccttt ctttcagggc ttttcggctg ttggctacac tgatgtgacc 360 cccctccctt tttggaatga tggggatctt tttggtgtat gttggatttg ttttcttttc 420 cgttttatat gtacaacaag ggctttcttc tcaagcaaaa tttaccgagt ttccgcggaa 480 cgtgacggcg accgaggggc agaatgtgga gatgtcctgc gccttccaga gcggctccgc 540 ctcggtgtat ctggagatcc aatggtggtt cctgcggggg ccggaggacc tggatcccgg 600 ggccgagggg gccggcgcgc aggtggagct cttgcccgac agagacccgg acagcgacgg 660 gaccaagatc agcacagtga aagtccaagg caatgacatc tcccacaagc ttcagatttc 720 caaagtgagg aaaaaggatg aaggcttata tgagtgcagg gtgactgatg ccaactacgg 780 ggagcttcag gaacacaagg cccaggccta tctgaaagtc aatgccaaca gccatgcccg 840 cagaatgcag gccttcgaag cctcgcccat gtggctgcag gatatgaagc cccgcaagaa 900 cgtctccgca gccatcccca gcagcatcca tggctctgcc aaccaacgaa cgcactccac 960 ctccagccct caagtggtag ccaaaatccc caaacaaagt ccacaatcag caaagagcaa 1020 atcgcctgta aaatctacgg agcggacagc aaagttgacc ctaaactcca agcaccaccc 1080 tgcacccact gtactctaat tcactacaca aggagcgcct gcttccggaa gcataaatga 1140 agaggctatc acatgctttg ttgatcatat tttctttggc aaaacactga tcttttattt 1200 taagagaatt aacgtgaagt gatagaacgt tttctaatag caagatctat tttttccctt 1260 ttctttcggc gactaaaatc atctcactga ctgctcaagg gttggcctga atgtcatcag 1320 gatagggaat atttactatg gataccacta atttcctact aaaggaccca gcatcttcag 1380 gaagcaaaca gagatcaaaa ggctacagaa cagaagctat catcagacaa aacccccttt 1440 ttaggggaag aacaaaacta tcaacactgc aagtcaacaa ggaggacatt actttaagga 1500 ataacatgag aaagaaattt ttttattttc cccttttttt cttggatttt tcttcttttt 1560 cttgattaca gttcttgttc aatggtggca agtgctggtt atggccaatc tccgtcaatc 1620 ctaggaggtt tatagaacta cattttgagt gttctatatt tcagtgtatt ttaattcatt 1680 ttgcaattcc tgtgtatgca aacctgataa attctgtaaa ttgcttatag tatgtgtgct 1740 ataacttcaa agtagatgta ctgcgaccct catgcaagct gatttttatc attatatata 1800 taaatatata cttaagaata tctgtgtgtt gggccaatga ccaacttttt ttgacgaagc 1860 atttgttttt cgttgataat tcatacactg cgtgaatttt gtaattcatt gtttcacttc 1920 cacaggtttg acagctgcag atggtctcta ttgtcctctg cttcattctg gaaagtgcat 1980 attcaaaatt gtatcagtct ctgatcgatg aattaatttt gttatgtctg tgctaagttg 2040 gaatttacta tgttccttta tacatggtgt ttattgaggt ttgagagtct cttgactgtg 2100 aagaatgtac actgtctggt tttgacagct atttctgtat tattatcatt ataatcttgt 2160 caaatagaaa tgttgcttct agaaaatttg cctaggaggc gaatgtgggg aaggtgaagc 2220 actcaccata attccctaaa ttcatgttag aacatttctt gctatggtta aaaatgctgc 2280 ttcctttgac ctttatgaat ttctgtacct ttgtcattct gttacctttg tcattctgtt 2340 atttgcgcta attatatttt aatgtctcct aattaaaaat taaaatttgg ttgttggcta 2400 aatacaatat gcaaaagatg atggcaggtc cccgactaaa gaagattaat gtgttcagtt 2460 ttcactggtt aagtgaatta taattttaaa tattccattc ttatttatgt ctttatgata 2520 attcagacta ttttattttg aacctgtttt ctactctggc aaagaaagat aggcagaact 2580 attagtgttc catatacatt atggaataga taaagcttga gagataaatg acctaagttt 2640 tccttccaga gagactcttc cattttctct cattacaaaa ccagaagatc agctatgtgg 2700 ggccatcagc tcccagccta aggtcctata acccgaagct tgaaggcaat cagtacctct 2760 gcttttcaaa ggtaaatgca ttcattttct ttgattcagt tataagcaag tatatatttt 2820 cataatattc ttgacattac ctgagaaata atacttcatg ctaaatcttt tactgccact 2880 tttctcattc atttggttta tcatttcagt ttaatgagaa aaattaataa aggttttgat 2940 tgcactattt taaaaaaaaa aa 2962 <210> SEQ ID NO 46 <211> LENGTH: 1638 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2891329CB1 <400> SEQUENCE: 46 ggggggatga ggtgggttgg gccgggccgg ttgctaagac ttggcgaagc gctgcgctcg 60 cgcccggatc cctcaggcgg ctgcaggctt cagcctgcgc tggttggtga aacagagatg 120 tcagaaaagg agaacaactt cccgccactg cccaagttca tccctgtgaa gccctgcttc 180 taccagaact tctccgacga gatcccagtg gagcaccagg tcctggtgaa gaggatctac 240 cggctgtgga tgttttactg cgccaccctc ggcgtcaacc tcattgcctg cctggcctgg 300 tggatcggcg gaggctcggg gaccaacttc ggcctggcct tcgtgtggct gctcctgttc 360 acgccttgcg gctacgtgtg ctggttccgg cctgtctaca aggccttccg agccgacagc 420 tcctttaatt tcatggcgtt tttcttcatc ttcggagccc agtttgtcct gaccgtcatc 480 caggcgattg gcttctccgg ctggggcgcg tgcggctggc tgtcggcaat tggattcttc 540 cagtacagcc cgggcgctgc cgtggtcatg ctgcttccag ccatcatgtt ctccgtgtcg 600 gctgccatga tggccatcgc gatcatgaag gtgcacagga tctaccgagg ggctggcgga 660 agcttccaga aggcacagac ggagtggaac acgggcactt ggcggaaccc accgtcgagg 720 gaggcccagt acaacaactt ctcaggcaac agcctgcccg agtaccccac tgtgcccagc 780 tacccgggca gtggccagtg gccttagagg gagcctgccc tgcccccacc gcccaccacc 840 tcctcccctt cattcctgct gctacccctg gtcccgaggg ctgggagtac ctggggcccc 900 atccccccag ctgggatggt ggaagccggt ggtggccacg gaccgccccc ctcctgccag 960 ggccacagaa cccgtgttca tctcatccga gagcggagtt cctcacaagc actccccagc 1020 agcccttggc ctctgccgtc cacaggacgc cctcttgctc ccggaaacgt gtggtcaccc 1080 gccgtccact gcacggctgg tacggccttg tcttcaggtc tcgaggcctg actccggggg 1140 acaggtggca gcaggtcggc cgccctcccg tcctccaaga gctgctggcg ctgaggtcag 1200 agcgggtctg atggggagct ccgtctcacc ggccacccgc cgtcaccatg gcagatgccc 1260 ttggccggaa ctaataagag gcgtcggggc cagcttccgg tcccctgcag tgatagaggg 1320 cttggtgcct agctgagtcc tcgctgtccc cgccatcccc tgatctgtgc ggctccagcc 1380 tcgccccctc cccacgtgca ccatacctgg ggagttcctg gtccagggta tcctggggcc 1440 accctccctg cctccaaaac agggatccct ggcaggctgt ctttccacgc ccctgagttc 1500 agagtcgggg acccaggcca ggtcgggagc acagccgctc cccaaaccca gcaaaccggc 1560 agagagccgg tttcccagca gccggagccc tgcaggagag gcctttgtgt tttgttttgt 1620 tttgtttttt ctcttttc 1638 <210> SEQ ID NO 47 <211> LENGTH: 3322 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7474130CB1 <400> SEQUENCE: 47 ggagacgcga gtgcggggtg gcgccggtcc acctccgcag cgctcctgcc tcccccaggc 60 tttggaaggc gggcccgggc tgcggcagcg gcggcctcgg ctgcctgggg agtcaccttc 120 aggccattca gaggaggaaa gagaggggaa tatgaagtca gccaagcccc aagtgaacca 180 cagtcagcat ggggaaagcc agcgggcctt gagccccctg cagtctactc tgagttctgc 240 tgcatctcct tcccaagcgt atgagaccta tattgaaaat ggactcatat gccttaaaca 300 caaaattaga aacatcgaga aaaagaagct caaactggag gattataagg atcgcctgaa 360 aagtggagag catcttaatc cagaccagtt ggaagctgta gagaaatatg aagaagtgct 420 acataatttg gaatttgcca aggagcttca aaaaaccttt tctgggttga gcctagatct 480 actaaaagcg caaaagaagg cccagagaag ggagcacatg ctaaaacttg aggctgagaa 540 gaaaaagctt cgaactatac ttcaagttca gtatgtattg cagaacttga cacaggagca 600 cgtacaaaaa gacttcaaag ggggtttgaa tggtgcagtg tatttgcctt caaaagaact 660 tgactacctc attaagtttt caaaactgac ctgccctgaa agaaatgaaa gtctgagtgt 720 tgaagaccag atggagcagt catccttgta cttttgggac cttttggaag gtagtgagaa 780 agcagtggta ggaacgacat acaaacactt gaaggatcta ctgtctaaat tgctgaactc 840 aggctatttt gaaagtatcc cagttcccaa aaatgccaag gaaaaggaag taccactgga 900 ggaagaaatg ctaatacaat cagagaaaaa aacacaatta tcgaagactg aatctgtcaa 960 agagtcagag tctctaatgg aatttgccca gccagagata caaccacaag agtttcttaa 1020 cagacgctat atgacagaag tagattattc aaacaaacaa ggcgaagagc aaccttggga 1080 agcagattat gctagaaaac caaatctccc aaaacgttgg gatatgctta ctgaaccaga 1140 tggtcaagag aagaaacagg agtcctttaa gtcctgggag gcttctggta agcaccagga 1200 ggtatccaag cctgcagttt ccttagaaca gaggaaacaa gacacctcaa aactcaggtc 1260 tactctgccg gaagagcaga agaagcagga gatctccaaa tccaagccat ctcctagcca 1320 gtggaagcaa gatacaccta aatccaaagc agggtatgtt caagaggaac aaaagaaaca 1380 ggagacacca aagctgtggc cagttcagct gcagaaagaa caagatccaa agaagcaaac 1440 tccaaagtct tggacacctt ccgtgcagag cgaacagaac accaccaagt catggaccac 1500 tcccatgtgt gaagaacagg attcaaaaca gccagagact ccaaaatcct gggaaaacaa 1560 tgttgagagt caaaaacact ctttaacatc acagtcacag atttctccaa agtcctgggg 1620 agtagctaca gcaagcctca taccaaatga ccagctgctg cccaggaagt tgaacacaga 1680 acccaaagat gtgcctaagc ctgtgcatca gcctgtaggt tcttcctcta cccttccgaa 1740 ggatccagta ttgaggaaag aaaaactgca ggatctgatg actcagattc aaggaacttg 1800 taactttatg caagagtctg ttcttgactt tgacaaacct tcaagtgcaa ttccaacgtc 1860 acaaccgcct tcagctactc caggtagccc cgtagcatct aaagaacaaa atctgtccag 1920 tcaaagtgat tttcttcaag agccgttaca ggcagcaatt cccccaggca agcaaccgtc 1980 ttcactagct tctccaaatc ctcccatggc aaagggctct gaacagggct tccagtcacc 2040 tccagcaagt agtagttcag taaccattaa cacagcaccc tttcaagcca tgcagacagt 2100 atttaacgtt aatgcacctc tgcctccacg aaaagaacaa gaaataaaag aatcccctta 2160 ttcacctggc tacaatcaaa gttttaccac agcaagtaca caaacaccac cccagtgcca 2220 actgccatct atacatgtag aacaaactgt ccattctcaa gagactgcac agacgaatgt 2280 gtttcccaga cctactcagc catttgtcaa tagccgggga tctgttagag gatgtactcg 2340 tggtgggaga ttaataacca attcctatcg gtcccctggt ggttataaag gttttgatac 2400 ttatagagga ctcccttcaa tttccaatgg aaattatagc cagctgcagt tccaagctag 2460 agagtattct ggagcacctt attcccaaag gtgtttggaa acatctgagc ctctttggtt 2520 gctggggaag gccaggataa tttccagcag tgttataagc gaggagggac atctggtggt 2580 ccacgagcaa attcgagagc agggtggagt gattcttctc aggtgagcag cccagaaaga 2640 gacaacgaaa cctttaacag tggtgactct ggacaaggag actcccgtag catgacccct 2700 gtggatgtgc cagtgacaaa tccagcagcc accatactgc cagtacacgt ctaccctctg 2760 cctcagcaga tgcgagttgc cttctcagca gccagaacct ctaatctggc ccctggaact 2820 ttagaccaac ctattgtgtt tgatcttctt ctgaacaact taggagaaac ttttgatctt 2880 cagcttggta gatttaattg cccagtgaat ggcacttacg ttttcatttt tcacatgcta 2940 aagctggcag tgaatgtgcc actgtatgtc aacctcatga agaatgaaga ggccttggta 3000 tcagcctatg ccaatgatgg tgctccagac catgaaactg ctagcaatca tgcaattctt 3060 cagctcttcc agggagacca gatatggtta cgtctgcaca ggggagcaat ttatggaagt 3120 agctggaaat attctacgtt ttcaggctat cttctttatc aagattgaaa gtcagtacag 3180 tattgacaat aaaaggatgg tgttctaatt agtgggattg aaggaaaagt agtctttgcc 3240 ctcatgactg attggtttag gaaaatgttt ttgttcctag agggaggagg tccttctttt 3300 tgtttcaacc gtcggcactg ct 3322 <210> SEQ ID NO 48 <211> LENGTH: 5278 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2109928CB1 <400> SEQUENCE: 48 gtttcaccat gttggtcagg ctggtcttga actcctgacc tcaggtgatc cgcccccctc 60 aacctcccaa agtgctggga ttacaggcat gaaccactgc gcctggactt ttattttttt 120 ttttaatata atttcttttt ttgtagagat ggtgtctctc tgtgttgccc agcctagtct 180 tgaactcctg ggctcaggaa agttgagcag attgttcaga gaactctcat ctataccacc 240 ccccatgcag agtttcctct attattaaca tcttactatg gtggttccag gaaagaaatc 300 actgaacact gggaatggct tgagcaaaat ctcttgcaga cactctccat ctttgaaaat 360 gagaatgata tcaccacatt tgtgagagga aaaatacagg gcatcattgc agaatacaac 420 aaaatcaatg atgtaaagga agatgatgac acggagaagt ttaaagaagc cattgtgaaa 480 tttcataggc tgtttgggat gccagaggaa gagaaactcg tcaactatta ctcttgcagc 540 tattggaagg ggaaggtccc ccgtcagggt tggatgtacc tcagcattaa ccacctttgc 600 ttttattctt ttcttatggg aagggaagcg aaactggtca tccggtgggt agacatcact 660 cagcttgaga agaatgccac cctgcttctg cctgatgtga tcaaagtgag cacacggtcc 720 agtgagcatt tcttctctgt attcctcaac atcaacgaga ccttcaagtt aatggagcag 780 cttgccaaca tagccatgag gcaactctta gacaatgagg gatttgaaca agatcgatcc 840 ctgcccaaac tcaaaaggaa atctcctaaa aaagtgtctg ctctaaaacg tgatcttgat 900 gccagggcaa agagtgagag ataccgtgca cttttccggc tgcccaaaga tgaaaaatta 960 gatggccaca cagactgcac tctctggact ccatttaaca aaatgcacat tttggggcag 1020 atgtttgtgt ccacaaatta catctgtttt accagcaagg aggagaactt atgtagcctc 1080 attatcccgc tccgtgaggt gacaattgtg gaaaaggcag acagctccag tgtgctcccc 1140 agtcccttat ccatcagcac ccgaaacagg atgaccttcc tatttgccaa cttgaaagat 1200 agagactttc tagtgcagag gatctcagat ttcctgcaac agactacttc caaaatatat 1260 tctgacaagg agtttgcagg aagttacaac agttcagatg atgaggtgta ctctcgaccc 1320 agcagcctcg tctcctccag cccccagaga agcacgagct ctgatgctga tggagagcgc 1380 cagtttaacc taaatggcaa cagcgtcccc acagccacac agaccctgat gaccatgtat 1440 cggcggcggt ctcccgagga gttcaacccg aaattggcca aagagtttct gaaagagcaa 1500 gcctggaaga ttcactttgc tgagtatggg caagggatct gcatgtaccg cacagagaaa 1560 acgcgggagc tggtgttgaa gggcatcccg gagagcatgc gtggggagct ctggctgctg 1620 ctgtcaggtg ccatcaatga gaaggccaca catcctgggt actatgaaga cctagtggag 1680 aagtccatgg ggaagtataa tctcgccacg gaggagattg agagggattt acaccgctcc 1740 cttccagaac acccagcttt tcagaatgaa atgggcattg ctgcactaag gagagtctta 1800 acagcttatg cttttcgaaa tcccaacata gggtattgcc aggccatgaa tattgtcact 1860 tcagtgctgc tgctttatgc caaagaggag gaagctttct ggctgcttgt ggctttgtgt 1920 gagcgcatgc tcccagatta ctacaacacc agagttgtgg gtgcactggt ggaccaaggt 1980 gtctttgagg agctagcacg agactacgtc ccacagctgt acgactgcat gcaagacctg 2040 ggcgtgattt ccaccatctc cctgtcttgg ttcctcacac tatttctcag tgtgatgcct 2100 tttgagagtg cagttgtggt tgttgactgt ttcttctatg aaggaattaa agtgatattc 2160 cagttggccc tagctgtgct ggatgcaaat gtggacaaac tgttgaactg caaggatgat 2220 ggggaggcca tgaccgtttt gggaaggtat ttagacagtg tgaccaataa agacagcaca 2280 ctgcctccca ttcctcacct ccactccttg ctcagcgatg atgtggaacc ttaccctgag 2340 gtagacatct ttagactcat cagaacttcc tacgagaaat tcggaactat ccgggcagat 2400 ttgattgaac agatgagatt caaacagaga ctgaaagtga tccagacgct ggaggatact 2460 acgaaacgca acgtggtacg aaccattgtg acagaaactt cctttaccat tgatgagctg 2520 gaagaacttt atgctctttt caaggtgagt tgcaaggcag aacatctcac cagctgctac 2580 tggggcggga gcagcaacgc gctggaccgg catgacccca gcctgcccta cctggaacag 2640 tatcgcattg acttcgagca gttcaaggga atgtttgctc ttctctttcc ttgggcatgt 2700 ggaactcact ctgacgttct ggcctcccgc ttgttccagt tattagatga aaatggagac 2760 tctttgatta acttccggga gtttgtctct gggctaagtg ctgcatgcca tggggacctc 2820 acagagaagc tcaaactcct gtacaaaatg cacgtcttgc ctgagccatc ctctgatcaa 2880 gatgaaccag attctgcttt tgaagcaact cagtacttct ttgaagatat taccccagaa 2940 tgtacacatg ttgttggatt ggatagcaga agcaaacagg gtgcagatga tggctttgtt 3000 acggtgagcc taaagccaga caaagggaag agagcaaatt cccaagaaaa tcgtaattat 3060 ttgagactgt ggactccaga aaataaatct aagtcaaaga atgcaaagga tttacccaaa 3120 ttaaatcagg ggcagttcat tgaactgtgt aagacaatgt ataacatgtt cagcgaagac 3180 cccaatgagc aggagctgta ccatgccacg gcagcagtga ccagcctcct gctggagatt 3240 ggggaggtcg gcaagttgtt cgtggcccag cctgcaaagg agggcgggag cggaggcagt 3300 gggccgtcct gccaccaggg catcccaggc gtgctcttcc ccaagaaagg gccaggccag 3360 ccttacgtgg tggagtctgt tgagcccctg ccggccagcc tggcccccga cagcgaggaa 3420 cactcccttg gaggacaaat ggaggacatc aagctggagg actcctcgcc ccgggacaac 3480 ggggcctgct cctccatgct gatctctgac gacgacacca aggacgacag ctccatgtcc 3540 tcatactcgg tgctgagtgc cggctcccac gaggaggaca agctgcactg cgaggacatc 3600 ggagaggaca cggtcctggt gcggagcggc cagggcacgg cggcactgcc ccggagcacc 3660 agcctggacc gggactgggc catcaccttc gagcagttcc tggcctccct cttaactgag 3720 cctgccctgg tcaagtactt tgacaagccc gtgtgcatga tggccaggat taccagtgca 3780 aaaaacatcc ggatgatggg caagcccctc acctcggcca gtgactatga aatctcggcc 3840 atgtccggct gacacgggcg ccttcccggg ggagtgggag gagagggagg ggagggattt 3900 tttatgttct tctgtgttga gttttttctt tctttctttt aaattaaata tttattagta 3960 cctggcttga agcctagtgt tttcataatg taattcaatg aaaactgttg gagaaatatt 4020 taaacacctc aatgtaggta cattacactc ttgttgcggg gaggggattt accagaatac 4080 agtttatttc gtgaattcta aaaaacaaaa agatgaatct gtcagtgata tgtgtgtatt 4140 ataacttatt aatcttgctg ttgagctgta tacatggttt aaaaaatagt actgtttaat 4200 gctaagtaag gcagcagtca tttgtgtatt caggcttttt aaataaaatt agagctgtaa 4260 ggaaaatgaa aagccacaaa tgcaagactg ttcttaaatg gaaggcatag tcagcgaggg 4320 taaatcctat accactttag gaagtattaa aaatattttt aagatttgaa atatatttca 4380 tagaagtcct ctattcaaaa tcatattcca cagatgttcc ccttcaaagg gaaaacattt 4440 ggggttctaa acagttatga aagtaagtga tttttacatg attccagaat aacacttgta 4500 ttgaccaatt tagacagata ccagaccaat tttgcattta agaaattgtt ctgattattt 4560 acgtcaactc attagaattc agtgaaaagt aacagtcttt tgtcacagag aatctgaaag 4620 tagcagcaaa gacagagggc tcatgacagg tttttgcttt tgctttgctt ttgtttttga 4680 aagagtaaaa gtactgatgc ttctgatact ggatgtttag cttcttactg caaaaacata 4740 agtaaaacag tcaactttac catttccgta ttctccatag attgaagaaa tttataccac 4800 atatcgcata tgaccatctt tccatcaaat caatgtagag ataatgtaaa ctgaaaaaaa 4860 atctgcaaga taatgtaact gaatgtttta aaaacagaac ttgtcacttt atataaaaga 4920 atagtatgct ctatttcctg aatggatgtg gaaatgaaag ctagcgcacc tgcactttga 4980 attcttgctt cttttttatt actgttatga ttttgctttt tacagatgtt ggacgatttt 5040 ttcttctgat tgttgaattc ataatcatgg tctcatttcc tttgcttctt tggaatattt 5100 ctttcaacac attcctttat tttattatac attgtgtcct ttttttagct attgctgctg 5160 ttgtttttta ttctatttac aggatgattt ttaaactgtc aaatgaagta gtgttaacct 5220 caaataggct aaatgtgaac aaataaaata cagcaaatac tcagatacaa aaaaaaaa 5278 <210> SEQ ID NO 49 <211> LENGTH: 1282 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2675716CB1 <400> SEQUENCE: 49 tccccattca gggcgccaaa ttttgggaag ggccaaccgt tcggccccct tcgccatttg 60 cccaacttcg caaaagggga tttcccccaa agccgtttaa ttcggttacc ccagggtttt 120 cccagtcacg gccctttaaa accgccgccc ctgaaatgaa attagggggc accttggaag 180 ggcctttacc tcccattcac cccttcccaa acctggaacc ccctgggccg cccccccttt 240 tttttttttt tttttttttt tttttttttt tttttttttt tttttttttt tttttttttt 300 acagcgatga gataaacatg tatttgttga catggaaaga ggttcacaat gtacagttaa 360 gtgcaaaagc agattataag aaaacagtgt gcatagtagg ataccacggt ggcaaaatct 420 atattctata tattcataga aaaaggccta gaagaaaata taacagtatt caccccagag 480 agtgggatgg ccaatgagtc ttctttctgc ttctattttc taatctttct acaatgtttg 540 tgtagtcagt tttcctggtt tgcttttttt tttttttttt ttttgagcac aggtgggtca 600 tgggagtcac gctctcatgc tgcctgtcaa gagcatggta cttgctacag gggctactcc 660 ccagcagctc tgcttaagaa gattctggga atgtcttgag tctccagaac aaggaacaag 720 cacttcctgt gcccagggaa ccagcagctt cccacttctt ctcacagcaa ccttgtgggg 780 ttgaggtttt ctgtctgctt gatggaaaag aagagcccag agaggggagg tacctgccta 840 agttcacaca gcagggattt aaagccgggt cacctggccc agagccccgg gggctattaa 900 agcttatgaa cagagcaagc agctgagccc agggaagggc tcaacattct cccgtgattt 960 ccgctgtgtt gacaagctgc aaatgtgcca ggaaaggact gggtgtggtg gctcatgcct 1020 gtaatccccg cactttggga ggctgaggtg ggcggatcac ctgagctcag gagttcaaga 1080 ccagcctagg caacatggca aaacctcgtc tttactaaaa atacaaaaaa ttagccgggt 1140 gtggtgacgc accctgctac tggggaagct gaggcaggag aactgcttga acccaggagg 1200 tggaggttgc agtgagccaa gattgcacca ctgcactcca gcctgggcga ctgaacgaga 1260 ctctgggtct caaaaaaaaa aa 1282 <210> SEQ ID NO 50 <211> LENGTH: 1550 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1953366CB1 <400> SEQUENCE: 50 gcgcccagat ggttcttcca tgtgaagttg tctcgggctc tgggctgacg agagaacacc 60 tggtaaccag gttagccctc tgtcagtcac ccagggcagg gcagcatggt gcggattcag 120 aggaggaagc ttttggcatc ttgcctgtgc gtcacagcca ccgtctttct gcttgtcaca 180 ctccaggtca tggttgagct ggggaagttt gaaaggaagg agtttaaaag ttccagtttg 240 caagatggac atacaaaaat ggaggaagca cctacgcatc ttaattcatt tcttaagaaa 300 gaaggattga ccttcaacag gaaaagaaaa tgggaattgg acagctaccc cattatgctc 360 tggtggtccc cgctgacggg ggagactggg aggttaggcc aatgtggagc agatgcttgt 420 ttcttcacca tcaaccggac ctacctccat catcacatga ccaaagcatt cctcttctat 480 gggcttacca cccaaaagat gggaggcaga agatacccac ctgagttgcc cagagcccac 540 agtgtttgct ttctcaccac tccggactcc acctttgagc tctttgcgag agatgtggat 600 ttccagcttt gaacaatcca agaaagaagc ccaggcacta aggtggctgg ttgataggaa 660 tcaaaacttt tcatctcaag agttttgggg cctagtattc aaggactgat ttcaaaaatg 720 atcagaatga aacagactag agccttcttg aggtttattt tctaggttgc cttaatattt 780 gaacataata gctattctgt tgactatcca tcaggataat aattagttgc tgcagtactc 840 ataatgagcc ctttcaagga atagatgtaa attaccctta ggggtagcca ctatattttt 900 tatactaaaa aaggaaatat ttcttatgga cactggttat cttccatgtc cgtgtctgtg 960 gacccacata cttactgcct tttgtggaaa ttcacctaga gtgagtactt tccttgtgca 1020 atggagggag acgatctagc tatagattct tgatactcac ctcactctca acagcttatt 1080 ggtatttggc aaacctggta tcctgcagcc gagcatgaac atgaaataca ttagaacttg 1140 gcaatgagag atcccatctg ttggtttcca gggatgtaag tgagtaataa aagctgtttc 1200 aagtttatcc actatccact cttcaagtga aaagaactta tgtgtgtcta ccttcttctc 1260 cataccctga gccacctctc tcactttctt tagttgtgcc ttgccctatc gcctcccatt 1320 ttcccttcaa agtagaatgt cttgtaaaga cacagtaact cctgtgtgtt ttgattagtg 1380 agatgttacc acttacccct tctgctgcgc agaataatat taagaattgc tatgcttatg 1440 attcaggctg gacagcctgg acattttgag cagcgcgaga gtagaagtga atacccccag 1500 gaactccaat tgtgctgaag ctgatttgtc tgttcgtagg atgatgtgca 1550 <210> SEQ ID NO 51 <211> LENGTH: 1543 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3992330CB1 <400> SEQUENCE: 51 cttaatataa atgtaaattt attttttaat tatttggtat aatgccaagg tctttacttt 60 gagcgagtct attaattgta gttttctgtt atctttcatg cataaactat gtatgtttaa 120 ctcattcttt ataatttcca gtttaaattt ctttgaagaa gagtgagaac tgagagatca 180 ttttgatctc ctttcaatct tctatggttt tatagttttt ctgacttttt ataattacct 240 tacctacctc taattaaata gcagtgaatt taaaaacaca tctgtgctgg gcctttcaca 300 ttcagtttag gtgttacaga aaaactaact ctttatactt ttatttatta ctttgaggca 360 tacgtaatta aattgtgcaa ttataataac aggttgtggc aaatatgata gattggctta 420 acatctgttg caccttcctt ttaatatgcc ttcctgtatt gcagaggctg gaaaactaaa 480 aactagttca ggatatgggt ttggttctgc taatgataac cacttgtacg atacctaaat 540 tgggaaatag tgggagaaaa ggcagtgcct gaggcatcta ttttgtggct aagaatctaa 600 gaagcgtagt atggctgtag agccaacaat tctggcagtc acttctgtca aagctaaggc 660 agggtgttgc tgcaggcagc agctctggca ataacattct ggtctcagga tctcagcaaa 720 gggatgtgat tctagaacca gcagtagata tagctgcttc ctgattgtcc agtttcctaa 780 ttgtgaccaa tgtagcaaac catttctaca attagctaaa tcagtaagat tgactttttt 840 tccagaactt acactggaac atagagatca gctaattgat agtgatagca gaaaagaagt 900 tatgcagaga tatatggtgc tattagtgtt attaataata cagataacac tgtttgcctc 960 caaaacgttt tatttaattt ctcttcttaa tatcaagcca accaaatata atagtacttt 1020 ctctttttta ttttcctttg gctcttacat tttgacttgc ttatgtattt taataaatac 1080 aactggaacc aaaattgtct tactatcttg catataatat ttttttagat atttgttgag 1140 cttgaattgt tgatatttaa ttttcaagat gtttaaccat acataaaaaa taatgcttta 1200 agtgatttct taaaccttta gggtacttaa ctgattttct taattatact gccaatatgt 1260 tggaaaatca gataaaattc atttgatctg tatttattta caaatatatt attacaactg 1320 ttatatttaa aagaaaacaa gaaaataagc aaagatagat gatataagga gcaaataaca 1380 agtttgatta tgtacatgta catttctgtt tatacacact catatattaa ccaacaggaa 1440 tatactttgt ttttcaaaga cccatgaaaa actcacaaac atagatatgc actgaaaacc 1500 ctccctacca catacacaca taacctattc ccccgagaaa aaa 1543 <210> SEQ ID NO 52 <211> LENGTH: 1531 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 4043652CB1 <400> SEQUENCE: 52 tgctttgttc actgcttatt aaaatggaaa tcctggagaa tagtagttct ggaatattgc 60 cgggtgaaag tccaattgtc atcacaatgt tatatattga caccccagtg tcatcagtca 120 ggcaggagcc aaacaatgaa tgcccctctt aggtattccg cctgggattt tgttttgtct 180 gttccctaag aaaatatatt ttcattcctg caaacacagt gctcagcctt cagttccctt 240 ccacttgagt tctctcttct cctgctggaa gccgcccctc tctgcgatgg acgtgaggac 300 gtgtccagct ctgctctgtg ggaaggagtt ggaatgttcg acagcagtgt tttctctcct 360 tttctgggcc tcctcgcaaa tgcccaggcc ctgcattttc acgctgtgct aagcagcctt 420 tggtctgcat gggggatggt gtgctcccag cctgcagtct ttggagcaag gctgctgccc 480 gtgccttggg tgctggagtt ggaggaggct gttctcagcc ctttcccttt tctgaaagct 540 gttcctggcc gggcatccca gggaagaagg aggggactgc gtgtatctcc tccacctctc 600 ccattccatc cccagtccag cctgggcaac cccacccctg ggagggatga ggcaccctct 660 tgctcagcct gctcagcctt ctctgagcct ttgcagggat ctgcagactc ctgagggcta 720 gaggacagag aaagagaata gaatgaaatg actttgattc ctgcgccttt tagttttgaa 780 ctctggaatt cctctgcccc ctccccaaca tttttttgga atctcaccct gttgcaaaac 840 tagagccatg tcccaagcat ctcacaaagg aataactgct ctgagcagag atgagtggtg 900 gttggcaggg gcaggcaact ttgggtgctg ctgatgcctg caaaagccat ttatggcttg 960 tggtgggggg cacatagatt ccccggtggg ttagacagga agtaactgat atcacttcac 1020 ccaaatatat aaccgtgatg gttatctatt taatttcagt ttttgttaac gagcgtgtct 1080 tactaaaacg ctccactttg agctccccca ccccctccag gtcctcagag tttgcagatc 1140 tgggctttct aaagcaagtg acctgaaggc tctgggctca ccatacaaca cccacgttgt 1200 ttatttcaaa gaacttttca gcgaagggag aggagctttc agaaaaacct cactctttcc 1260 cctcccttct cccctctttc cttctgccgg tccttttggc tggggtctga gtctgcggtt 1320 ctcgcctggg cagtcttgac gaggagcaaa ccccgccttc agagggcaga caaagcaggt 1380 ggcatgaatt gatcagcgag aaaggtgtga gccgaggcag ttcctgcgtt ctgctacaaa 1440 aggaatggaa agggaaggga atttcccccc accatgggct gtgggagagt tgaccgtatt 1500 ctgggcaaga ctccatgacc cctctgattc t 1531 <210> SEQ ID NO 53 <211> LENGTH: 922 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5540353CB1 <400> SEQUENCE: 53 ggagtttttg agaacctcat gaatttttat gcaaaattcc atgtacctct gtattctcca 60 atgcagtggt tcatggcatc atttgtgggt tccaaaaagg acttatggct cctcagaaca 120 aaataaacac tgatttgata ttcaaagggg gagcagaaag agagggcgcc agcgatgtta 180 ccaggtgcta ggccatgcag ggcctcataa gccatagtaa gtggcttgac ctcctctatt 240 ctgaagggag tgggcatcaa gggactggag atgagacgtg tgagaaaaac tggctgagaa 300 cagaggaaga gcttccccat ttgcattccc ttgaggtctg gagttgtgga agaaagccaa 360 ggaggtccct atttaccaac ccagattcct aggcattacc aggagaggcc agcagagggc 420 gctgtagccc agcatatgga catgaaggga aggggacttt ccagactaaa ggccctgcca 480 cctcctctct ggcgcattct agggtccctt ttagccacca accttggttc cttctcacgt 540 tctgatgccc tacccgagat tctgagacta gtcagtttcc ctcccttgtt tttgttgccc 600 atctcccctt cacaaggctc tgagctccca ccaggaagat tggggctgaa ttggcttctc 660 ctgtggccca gcattgtctc tcacaaggag ccaggaacac agcatgtatg agggaacgaa 720 gacataaggt tgctaaggaa gggggaagat gggccatggg gatgcaatct ggagtctttt 780 accctggtca ctcctccagg aagcctccct ggacacaccc caggctctca aagtgacact 840 tgggctggag gtcttgtctc tcggaggggg ccctggagac gggtccggac gcgtgacaat 900 aatgccagaa aggcagaagt ga 922 <210> SEQ ID NO 54 <211> LENGTH: 1378 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 5632328CB1 <400> SEQUENCE: 54 gttttctcat ctatagatat ggataatagc tgtgcccttc tcagaggtcc ccccatgtgg 60 gatttaaatg aaataattca tataaagttc ctagatcttg gcctagcacc tattatttta 120 ttgtctctct tctccagccc caaacctgct catgctgcag tctccccggt cctggtttgt 180 ggctcagtgg ttcacccagg ccaccctgtg tcctgcccgt gcccatatct agtcatctct 240 aggccgcagt ccttgctgcc tctgcattcc tgcggccctg tgttagttta gggcctcttt 300 ctctcttttc tgtagtagtg agttcctagc tcctgagcca gctgcatgat gcagtcccca 360 aatctgatac aatcctaata caacggccca atccgatcat tacaaaaagg cggaggagct 420 cgctatcaac tccagaatca agtccacaac ctccaaggtg tgcgcagcct ggcgagacct 480 gggctttgct cacccttctg gcttaattct taccacacac tcccctgtag cagccatgcc 540 aaaccacggc ccacgcttcc gtctccttgc ctttgttcgt gctgttcctg ctttctgctt 600 tacacctttc ctgtatcctt ctttacctgc tagatgcctg ctttgccatc aagacaataa 660 tcttttttaa atttaaattt aaattctttt gacttttagg tgtagggtac atgtgcacat 720 ttgttaggta aattgcatga aagacaatct taaatacatt tacagaccca gtagccagac 780 actgtactaa ctgtgattta catgtattca tataatcttt tcaacaacct cttgaagtgg 840 gtaccattta taaatgagga aactgaggca cagagaggtt ggtaagttga ccaagctcat 900 agaattagta actggcagag cctgggtgca aacccatgca gccagtgcta gaacctgcgc 960 ctgactgcta cgctatgtct caagcccctc gtaggcactg ccctcccact gatgcccacc 1020 tggcctcccc aggcactgtt tggtgcctcc cctttggtgc tggtgactac tgttgctttg 1080 ccacaacatg tgttagtcac agtgcttttt ccggcgaacc tctggagggc aaggaccgtg 1140 ttctgttcat tctcacatcc ccatggccca cagtgcttgg cacctggtag gtgcccaata 1200 gacgtttgtt acaccaaaag agctggtgaa tgaaatgtca tctgtaggac ttgtcagaat 1260 gccttcttgc ttccatcaac ctttggccct ccatttccaa gacttaccta agacttgcct 1320 ccttcctgaa gcctcaccca ccctcactct cttcctttgc tggaagcctc ctcgctcg 1378 <210> SEQ ID NO 55 <211> LENGTH: 900 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6727209CB1 <400> SEQUENCE: 55 cttttcccca atctgttcct tttcaacccc aaagtcatta tctaggccag cctcttatca 60 ctaatttcaa tggacttgat gacgtagttc tgggttctcc ctgagaaacc caccttaaca 120 tccatcacaa aatattttgg agttcccagt tggtcttcca catgtactca agaaaatgtc 180 tattcctatg gtctctgtgt tactctgcca ggcaccattg ttaatccaag tagctctgcc 240 aagaacagta gctataagga agaagagatt gtgcttagtg gacagcattc ttcaaacatg 300 gcatcttttc aacttttttt tagtaggctt tatttttcag agcatcttta ggttcacagc 360 aaaattgagt gaaagtacag agatttccca tttattcttt gccccaacac atgcaaaacc 420 tcacctgtta ccaatatccc ccaccagaga ggtacatttg ttataatcaa taaacctaca 480 atgacacatt gctatcaccc aaagtccata gtttacatta gggttcattc actcttcgtg 540 ttgtacattc tatgggtttt gacaaatgtc ataacatgta tttataatta tagaaatatg 600 tagaagagtt ttattgctct aaaattcctc tgtgctccat ccattcatcc ctttcttctc 660 ccagtctctt gaaaccactg ctactgttac ggtctccatg gttttgcctt ttccagaatg 720 tcatatagtt ggaatcatac cgtaggaagc cttttcagat tggctttttt cgcttagtaa 780 tatgcatttt aggtttctcc atagcttttc atggctaaat agctcatttc cttttagtgc 840 taatattcca ttgtctggat gtaccatagc ttatttatac tgcttattta ctgatgcatc 900 <210> SEQ ID NO 56 <211> LENGTH: 1152 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6923150CB1 <400> SEQUENCE: 56 gggattactt agaggtatga attgagagag aatacaagag gactaaggac aaagctcagg 60 gtcactccaa attttgtaag tcttcatttg gagatggaac atcctaatat ttttaagata 120 ccgacttaat atttgcaccc aagttaaaga ttcctcttga tcagaatgaa caggaagctt 180 taagctaagc acagtgctac caagaagcac catgttgacc ttgaggactc tggcaggaag 240 ctgtttgtgg ttgtcacacc tagtttcctc tgtgaaacta ctgctgcctg tgggtgatgt 300 ggttatatgc tgctggctgc tgttgattct cctgtttgtg tacaaggtgt ttttccctcc 360 cagtgcctcc caatgtaggc atcggttcat gcacagtgaa gtagttggct gcaagaaacc 420 ttgtaaggca gggagcagcc ttttgaatgc aataatctac ccaatcattt tattgactta 480 attatagaat gaatttcttt gaaacaaagt gaaagtctta gttgtattac actttaagac 540 atagagaaaa catgtaggtt tgtttctgta tacagtaaat ttctgtgctt ttctatatct 600 tatgaaactt gaatagttgg ctctgttgcc aggtgaaagt tttgctaggt tttttaaaaa 660 attagaataa gtacatttaa tacacaggga aattttatct tgaatattaa aagacattgt 720 taagctatct taacctttca gagtttattt gaaaaatcag aaagatgttt tactggctcc 780 tttgacacca agtcacatct tctccatatt tattgtcaag aatgttgact ttaacttatt 840 tctctgaaga cctgtctacc ttagggggag aacctgtgat agattctggt aaccaaggta 900 gaggaggggc aggaagacca atgaaggctg ttctgcatca gttgcctttt tagggaatgt 960 tcaacttatt atctgtctct gaagcaaatt tgaatatttg gatggtgggt gtattaattc 1020 attttaacgc tgctgataaa gacatgcccc aaactgggaa cataaagagg tttaattgga 1080 cttacagttc cagcatgact ggggagtcct cagaatcatg gtgtgaggcg aaagcacttc 1140 ttagtggcgt gc 1152 <210> SEQ ID NO 57 <211> LENGTH: 1423 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2589084CB1 <400> SEQUENCE: 57 ccgctgtccc ctccaacaca gtaaatctcc ttctattatt ctccaacttg tagtaagctg 60 tgtcattttg agaagaaata cataatggta tattagaaga atcatggatc ttctcattca 120 tgcttagaaa aaaatttatt acaatgtaag aaagtctgaa tagcatgaat ttattataat 180 gatttaacac ttctagcact cgagttaaaa atgcccttcc ataaataact gtccctggaa 240 aacatagcaa atttacacag tttaccattt cccaatgtta tataaatcca acaagcttaa 300 atcacctgca gctgagagaa gaacagagga aaccagagct gtgaagttca tcccatccca 360 atgggcagca atgaggagtg agagccagtc tcccctcctc cagctccctc atctcagcat 420 gggactggcc aatctcagca ctcaaagaat ggggagaaga acagggtggg gcagtacctg 480 gaagaatcaa ggagggcaaa caccacagtc ttacagctgc agaacaggtg aagggcacgg 540 gcctagggca tcctggaaga cgtcaggcca tgggccattg tttgtgtgct ggtgccaagg 600 aggtgtcagt taaggctgct cagctgtggc ctgcaaggaa gaagggaggg agaggccagc 660 tctgatgtcc tggtcagatc ttgaacaggg cctgtcctct ggccaaccac ctcttctact 720 ttcttacaaa tgccaacgct gctttctact cctgggcctt ctggatcctc cgtgttccaa 780 ggacctccct cttggcactc cctctggctc cactggacac cctcctcacc ctactttcat 840 ggacactgtg gcctcatcat tcttgctttc atctgggcta gtttccagat ctaggtcagc 900 attccaggca ccaaacctgt aaggcagaaa tggtcacttc tcatcttaat aaatattttt 960 atgcattatt atattcgagg cttagagaat ataggcaact tgcctaaatc tacacagctc 1020 acaagtggta aggctgggtt ctccaaagtg aatatatgtt ttctttgaac actttacatt 1080 ctaatagggc agacagtgca cagagcaata tgggacagat tgaggtgggc tataacaaag 1140 gctctacaga gtactatggg agccaagagt atataatgat gcctgagaga ttaggaaacc 1200 tccatggaag tgatgataac tgagcaaggt ctggaaagat tcatccaaaa tagagggacc 1260 tggaaaagtc acataggcag gaaacagcag catgtccttg ggagacggcc aagagttgtg 1320 agctgcagag gggagaaggg aggggcaaga tgctgacagt tccggtgtgc cactctaagg 1380 ggtgcactcc tttcctgtaa gcagtgggga acttgtgtat ttt 1423 <210> SEQ ID NO 58 <211> LENGTH: 1057 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7950559CB1 <400> SEQUENCE: 58 ccgcctcctc agcataccaa agtgctagca tcacaggtgt gagccaccac acctggctcc 60 atagtatttt cttatagcca tttttactgt ggagtagtaa tgtcccgact ttcatttcta 120 attttactta tttacatctt ctttcatttt cgggaagttc agttaaaggt ttgacaactt 180 tgatcttttt ccaagaagga accattggtt tcatagattc tattattttt atattatctg 240 cttcacatat ctatacccta atattgattt ccttcctctg gtagctagta gtttgctttt 300 tcctttttcc ttaaggtatg aacatgttat taattgaaga tctttcttat cttataatgt 360 atttacaaat attcattgct ctgagtttcc ttttactaca cccacaaatt ttgatatctt 420 tttttaaaaa attaacttca agttatgttc ttatttcatt cacattgtta aagccagtaa 480 gctataccag taatgtgggg ctgctgtctc cacaactatt gccaaggtgg acaatatagg 540 ataataggca ggtagtcaaa tgccacaatc cttagagaac tttagcagtc tcttcattct 600 aaactaagta gtaccctggg gtctctgttt atattagatt ccagagttcc aaaagagttg 660 atgttgttgc ctatttaatg gctgtttcaa tagaaactga ttcttggctc tccctatttc 720 tattttccat tacattactt cttgatctct tttaaaagtg cctcaacttt tccttcagtg 780 ttgtctagaa cagcagtccc caacttttct ggatgcaggt acaggtttca tagaagacaa 840 ttttttccac agacagggca gttgaggggc tggagggagg aggatggttt gggaatggtt 900 caatgcataa tatttatttt gcactttatt tctattatta ctacattgta atacataata 960 aaacaattat atgttcctcc gcagtcgact gtccttgttt atctctactt aaacgcactc 1020 gtctatcagc tggtcctttc ataacactca gttcaac 1057 <210> SEQ ID NO 59 <211> LENGTH: 688 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 6981966CB1 <400> SEQUENCE: 59 cctaaataag ttctactgat ggagctccaa gtgtcttagc ggcacagcac agccattaat 60 gaaacttaca agacagacaa tgcaattgtt acaaaaagcc tgggacttgg gaaatggtta 120 tgccagacct tccaaacctg actctaccgg ttagaatttt atgttgattt aagacaatat 180 aaatgaaagt ttaagtaaaa aaacattgag attggtggga agagatgaga ggcatctttt 240 ataaaataat ttataacttc ataaaatatg tgactaaaga attcttgcta atagagagtt 300 caataacatg aaattagaaa tactgagctt ttcagtattg aatctactgt cttgtgcaat 360 tctttttctt gtgcaaaagt atacatctcc ctgtaaaatt aaaaatgtaa taattccaga 420 caaaaatttc aaattgtgtt ctatgaaatc ctggagttgg agcaatagtt taaagaggtt 480 cattgaaata cagggtggtc acgaaagaca tgctttaaca ccaccaactt ggggagctga 540 tgctgacacg gaaagttatg ttggggctag aaaaataaac tgtgttctcc ggtttgggaa 600 gttagaggtg gtttagggaa cagcggctat ttttgggaaa ttggggcagg aaatttggga 660 aaaaagggtt tcttatgtgg gagaggag 688 <210> SEQ ID NO 60 <211> LENGTH: 1252 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1287125CB1 <400> SEQUENCE: 60 attaaagatg aaatacttga ccagaagcaa ccaattataa tagggattgt catccttcat 60 gtccagaact ggtttggtat gcaaatctga tcaaatcctc tgtgctttca tctctcagga 120 taaagcaaat tcttccatgt ggcccacaag actctgtggc ctggcccacc tgccttttca 180 gcatcttcct ccttattcac tctatcccag ctatcttggc ctcctgttca ccatgctccc 240 tcccaccagg gggctttgca tgttctccct gcctagaatg ttctcccttc ttccctttac 300 ctggtttacc ctcatgcttg gggatcgcaa ctcattcaac ccctcgtgac cttgatgggt 360 caaacccttg ctatgctctc agagcaccag acatctcttc ttagttgccc ttgtcacagt 420 tgcaatctta tacttattgt gtgattatat gattaatata tatttctctc tcgcatcaaa 480 ctataagctt cacgagggca ggttgccagt attgggtgcc tgttggtagg cacccaataa 540 gtacttatgg aatgaatgaa ccacgctgtg cacagtttaa tctttctttc atgattcaga 600 aggtagttca agaacctgta gtgcctcagg gtcataatta tgaacctcaa ttaggatctg 660 aaggtaaaag aggaaatgtc attggcagtc aattagccac aaggtagagc tagcctgaga 720 aagccagccc ctaaactcac caaaaataaa tctataatag ttgtcttccg tcacaccttt 780 gagtcaaggt gtggtatcct gaaagacctt gataaaatac ggataaatta gccagaaagg 840 acatcatact agctactcta taccaagagg agtatagtga ggtgaataag agcaaggact 900 ctaaagctgg acacacctgg cttcaaatcc cagctctgtc actttctgct ctgtgacctc 960 agccacaatc tctctgcttc atttttcttc ctcctctgta aatagagagg taaaagtagt 1020 atcttcatca ggggattgtt ggtaggggtt aaagacttcc tagatgtaaa gctcttagat 1080 cagtgcctgg ctcactgtaa gcacattttc atcatctcat gataaatcct gtacccatta 1140 gcagtcactc cccatttcta cctccttcca atgcctaaca accacaaaat tactttgtgt 1200 ctctatggat ttgtctatcc tggacatata aatggaatca tacaacaaaa aa 1252 <210> SEQ ID NO 61 <211> LENGTH: 1208 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2924950CB1 <400> SEQUENCE: 61 cggctcgagg cggcgcgatg gcggcggggc tggcgcggct cctgttgctc ctcgggctct 60 cggccggcgg gcccgcgccg gcaggtgcag cgaagatgaa ggtggtggag gagcccaacg 120 cgtttggggt gaacaacccg ttcttgcctc aggccagtcg cctccaggcc aagagggatc 180 cttcacccgt gtctggaccc gtgcatctct tccgactctc gggcaagtgc ttcagcctgg 240 tggagtccac gtacaagtat gagttctgcc cgttccacaa cgtgacccag cacgagcaga 300 ccttccgctg gaacgcctac agtgggatcc tcggcatctg gcacgagtgg gagatcgcca 360 acaacacctt cacgggcatg tggatgaggg acggtgacgc ctgccgttcc cggagccggc 420 agagcaaggt ggagctggcg tgtggaaaaa gcaaccggct ggcccatgtg tccgagccga 480 gcacctgcgt ctacgcgctg acgttcgaga cccccctcgt ctgccacccc cacgccttgc 540 tagtgtaccc aaccctgcca gaggccctgc agcggcagtg ggaccaggta gagcaggacc 600 tggccgatga gctgatcacc ccccagggcc atgagaagtt gctgaggaca ctttttgagg 660 atgctggcta cttaaagacc ccagaagaaa atgaacccac ccagctggag ggaggtcctg 720 acagcttggg gtttgagacc ctggaaaact gcaggaaggc tcataaagaa ctctcaaagg 780 agatcaaaag gctgaaaggt ttgctcaccc agcacggcat cccctacacg aggcccacag 840 aaacttccaa cttggagcac ttgggccacg agacgcccag agccaagtct ccagagcagc 900 tgcggggtga cccaggactg cgtgggagtt tgtgaccttg tggtgggaga gcagaggtgg 960 acgcggccga gagccctaca gagaagctgg ctggtaggac ccgcagggac cagctgacca 1020 ggcttgtgct cagagaagca gacaaaacaa agattcaagg ttttaattaa ttcccatact 1080 gataaaaata actccatgaa ttctgtaaac cattgcataa atgctatagt gtaaaaaaat 1140 ttaaacaagt gttaacttta aacagttcgc tacaagtaaa tgattataaa taccaaaaaa 1200 aaaaaaaa 1208 <210> SEQ ID NO 62 <211> LENGTH: 1077 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3471345CB1 <400> SEQUENCE: 62 cccgccgctg gcagccactc tcctggccgc caaaccccag ctggaactcc ggccacagcc 60 agcatgcagg gcgaagagag cctccggatc ctggtggagc ccgaagggga cagcttcccg 120 ctgatggaga tcagcacctg tgagaccgag gcctccgagc agtgggacta tgtcctcgtg 180 gcccaacgtc acacccagag agacccccgg caggcgcggc agcaacagtt cctggaggag 240 ctcaggagaa agggcttcca cattaaggtg atccgggacc agaaacaggt cttctttggg 300 atccgtgctg acaacagtgt ctttggcctg taccgcactc tcctcctgga gcctgagggg 360 cctgcccccc acgccgagct ggccgcgccg accaccatcc cggtcaccac gagtctcaga 420 atccgaatcg tgaacttcgt tgtcatgaac aacaagacct cggctggtga gaccttcgag 480 gatctgatga aggacggggt ctttgaggcc aggttccccc tgcacaagcc agggggaggg 540 acgcctgaag aagacgtggg cgcggtggag acacatgttc cgggagcagc cagttgatga 600 aatcaggaac tactttgggg aaaaggtggc cctgtacttc gtctggctgg gctggtacac 660 ctacatgctg gtgccggccg ccctgacggg cctcttagtc tttctgagcg gattctcgct 720 gtttgaggcc agccagatca gcaaggagat ctgtgaggcc cacgacatcc tcatgtgtcc 780 cctcggcgac cacagccgca ggtaccagcg gctctcggaa acctgcactt ttgccaagct 840 cacccacctc tttgacaatg atggcacggt ggtgttcgcc atcttcatgg ctctctgggc 900 cacggtgttc ctggagatct ggaagcggca gcgcgcccgc gtggtcctgc actgggacct 960 gtacgtgtgg gacgaggaac aggtgaggtg gagctggcag cgcagctgag gccgacccga 1020 gcaggggctg ttggcgcccg atgccctgca cggcccacat atgcctgccg tgtctga 1077 <210> SEQ ID NO 63 <211> LENGTH: 2053 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3615852CB1 <400> SEQUENCE: 63 cgcagctgca gatgaggagt tctgagaagc attgctcagg acagcggtaa atcacttctt 60 ggaggtgccc tgcacgccgg tcctgggagc aggcggcctc ccgggggtgc gggagcccca 120 ctcctccgtg gtgtgttcca tttgcttccc acatctggag gagctgacgt gccagcctcc 180 cccagcacca cccagggacg ggaggcatga gccggtcaag gcacctgggc aaaatccgga 240 agcgtctgga agatgtcaag agccagtggg tccggccagc cagggctgac tttagtgaca 300 acgagagtgc ccggctggcc acggacgccc tcttggatgg gggttctgaa gcctactggc 360 gggtgctcag ccaggaaggc gaggtggact tcttgtcctc ggtggaggcc cagtacatcc 420 aggcccaggc cagggagccc ccgtgtcccc cagacaccct gggaggggcg gaagcaggcc 480 ctaagggact ggactccagc tccctacagt ccggcaccta cttccctgtg gcctcagagg 540 gcagcgagcc ggccctactg cacagctggg cctcagctga gaagccctac ctgaaggaaa 600 aatccagcgc cactgtgtac ttccagaccg tcaagcacaa caacatcaga gacctcgtcc 660 gccgctgcat cacccggact agccaggtcc tggtcatcct gatggatgtg ttcacggatg 720 tggagatctt ctgtgacatt ctagaggcag ccaacaagcg tggggtgttc gtttgtgtgc 780 tcctggacca gggaggtgtg aagctcttcc aggagatgtg tgacaaagtc cagatctctg 840 acagtcacct caagaacatt tccatccgga gtgtggaagg agagatatac tgtgccaagt 900 caggcaggaa attcgctggc caaatccggg agaagttcat catctcggac tggagatttg 960 tcctgtctgg atcttacagc ttcacctggc tctgcggaca cgtgcaccgg aacatcctct 1020 ccaagttcac aggccaggcg gtggagctgt ttgacgagga gttccgccac ctctacgcct 1080 cctccaagcc tgtgatgggc ctgaagtccc cgcggctggt cgcccccgtc ccgcccggag 1140 cagccccggc caatggccgc cttagcagca gcagtggctc cgccagtgac cgcacgtcct 1200 ccaacccctt cagcggccgc tcggcaggca gccaccccgg tacccgaagt gtgtccgcgt 1260 cttcagggcc ctgtagcccc gcggccccac acccgcctcc accgccccgg ttccagcccc 1320 accaaggccc ttggggagcc ccgagtcccc aggcccacct ctccccgcgg ccccacgacg 1380 gcccgcccgc cgctgtctac agcaacctgg gggcctacag gcccacgcgg ctgcagctgg 1440 agcagctggg cctggtgccg aggctgactc caacctggag gcccttcctg caggcctccc 1500 ctcacttctg aaggtcccat cccctgctgc cctccgcagg cccagggctg ggcactccct 1560 gagacccaaa gacccacctc aacgacgagt ggcgttgagc cacttccctt tgaaaagaca 1620 ctcaaaatca ctgccatggt tcaatgttcc caggccccag gccatccact tgccggcccc 1680 caccagttct tgggttcccc gctctagttt gacctgtgca gcacattcca gaaggttcca 1740 gggaggttgt ggggcagcta gaggacaaaa tcatgaaaac agagtccctg tcttccagag 1800 atcatccggg gctttaatat taatggcccc caaaactccg taagaagcag gaaatgcagc 1860 ccaagtttta caaatgggta aacagaggca ctgagagata gatggtagtt tggtacttct 1920 ggttcccagt gcccaggaat ggtccactcc caagaaattc aggaaagaaa gactgaggag 1980 aaggtgtggg aacattctgg atgtttcggg agagttgggg aaactcctcc tcttaggaaa 2040 ggctaatact agg 2053 <210> SEQ ID NO 64 <211> LENGTH: 3250 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 4973984CB1 <400> SEQUENCE: 64 ggcgtgcggc ggagccgcgt cccctcagag gggcgctggc gcggggctga gccgcccggg 60 atcagcgcga gcacccagcc cgcctcggcc gggagggcag cgcggcactg cggggcgatg 120 agcggcgccc ggggcgaggg cccggaggcg ggcgccggcg gggctggggg ccgcgcggcg 180 cctgagaacc ccgggggcgt gctgagcgtg gagctgcccg ggctgctggc gcagctggcg 240 cggagcttcg cgctgctgct gcccgtgtac gcgctgggct acctggggct cagcttcagc 300 tgggttctcc tcgcgctcgc gctgctcgcc tggtgtcgcc gcagccgcgg cctcaaggcc 360 ctgcgcctgt gccgcgcgct ggcgctgctg gaagacgagg agcgcgtcgt gcgcctgggg 420 gtgcgcgcct gcgacctgcc cgcctgggtt cattttccag acactgaaag agcagaatgg 480 ctaaataaga ctgtaaaaca catgtggcct ttcatttgcc aatttataga gaagttgttt 540 cgagaaacta tagaaccagc cgtgcgggga gcaaacaccc accttagcac ctttagtttc 600 acgaaggtcg acgtgggcca gcagcccctc aggatcaatg gtgttaaggt atacactgaa 660 aatgtagaca aaaggcaaat tattttggac cttcagatta gttttgtagg aaattgtgag 720 attgatttgg agatcaaacg atatttttgt agagctggtg tgaaaagtat ccagattcat 780 ggtaccatgc gggtgatcct ggaaccgttg attggagata tgcccttagt tggagctttg 840 tctatcttct tccttaggaa accactttta gaaattaact ggacaggact gacgaatctt 900 ctggatgtcc ctggattgaa tggtttatca gatactatca ttttggatat aatatcaaac 960 tatctggtgc ttcccaatcg aatcaccgtt ccacttgtca gtgaagttca aatagctcag 1020 ttgcggtttc ctgtaccaaa gggtgttcta aggatacatt ttattgaagc tcaggatctt 1080 caggggaaag acacttacct taagggactt gtcaagggaa agtcagaccc ctatggaatc 1140 attagagttg gcaaccaaat cttccaaagc agagtcatca aggagaacct cagtccaaag 1200 tggaatgaag tctatgaggc tttagtgtat gaacatcctg gacaagaatt agagattgag 1260 ctctttgatg aagacccaga caaggatgac tttttaggaa gtcttatgat tgacctcatt 1320 gaagttgaaa aggagcgcct tttagatgaa tggttcactc tggacgaggt tcccaagggg 1380 aagctacact tgagactgga gtggctcacg ttaatgccaa atgcgtcaaa cctcgacaag 1440 gtgctaacag acatcaaagc tgacaaagac caagccaacg atggtctttc ctctgcattg 1500 ctgatcttgt acttggattc agcaaggaac cttccgtcag ggaagaaaat aagcagcaac 1560 ccaaatcctg ttgtccagat gtcagttggg cacaaggccc aggagagcaa gattcgatac 1620 aaaaccaatg aacctgtgtg ggaggaaaac ttcactttct tcattcacaa tcccaagcgc 1680 caggaccttg aagttgaggt cagagacgag cagcaccagt gttccctggg gaacctgaag 1740 gtccccctca gccagctgct caccagtgag gacatgactg tgagccagcg cttccagctc 1800 agtaactcgg gtccaaacag caccatcaag atgaagattg ccctgcgggt gctccatctc 1860 gaaaagcgag aaaggcctcc agaccaccaa cactcagctc aagtcaaacg tccctctgtg 1920 tccaaagagg ggaggaaaac atccatcaaa tctcatatgt ctgggtctcc aggccctggt 1980 ggcagcaaca cagctccatc cacaccagtc attgggggca gtgataagcc tggtatggaa 2040 gaaaaggccc agccccctga ggccggccct caggggctgc acgacctggg cagaagctcc 2100 tccagcctcc tggcctcccc aggccacatc tcagtcaagg agccgacccc cagcatcgcc 2160 tcggacatct cgctgcccat cgccacccag gagctgcggc aaaggctgag gcagctggaa 2220 aacgggacga ccctgggaca gtctccactg gggcagatcc agctgaccat ccggcacagc 2280 tcgcagagaa acaagcttat cgtggtcgtg catgcctgca gaaacctcat tgccttctct 2340 gaagacggct ctgaccccta tgtccgcatg tatttattac cagacaagag gcggtcagga 2400 aggaggaaaa cacacgtgtc aaagaaaaca ttaaatccag tgtttgatca aagctttgat 2460 ttcagtgttt cgttaccaga agtgcagagg agaacgctcg acgttgccgt gaagaacagt 2520 ggcggcttcc tgtccaaaga caaagggctc cttggcaaag tattggttgc tctggcatct 2580 gaagaacttg ccaaaggctg gacccagtgg tatgacctca cggaagatgg gacgaggcct 2640 caggcgatga catagccgca gcaggcagga ggcgtcctct tcagcgtagc tctccacctc 2700 tacccggaac acaccctctc acagacgtac caatgttatt tttataattt catggattta 2760 gttatacata ccttaatagt tttataaaat tgttgacatt tcaggcaaat ttggccaata 2820 ttatcattga attttctgtg ttggatttcc tctaggattt cgccagttcc tacaacgtgc 2880 agtagggcgg cggtagctct tgtgtctgtg gactctgctc agctgtgtcc gtaggagtcg 2940 gatgtgtctg tgctttatta tggccttgtt tatatatcac tgaggtatac tatgccatgt 3000 aaatagacta ttttttataa tctttacatg ctggtttaaa ttcagaagga aatagatcaa 3060 ggaaatatat atattttctt ctaaaactta ttaaattcgt gtgacaaata atcattttca 3120 tcttggcagc aaaaagttct cagtgaccta ttttgtggtg tttctttttg aaaagaaaag 3180 ctgaaatatt attaaatgct agtatgtttc tgcccattat gaaagatgaa ataaagtatt 3240 caaaatatta 3250 <210> SEQ ID NO 65 <211> LENGTH: 1399 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2122511CB1 <400> SEQUENCE: 65 gtcgcgccag cccgggcagg cagctttgca agtccgcgtt atatatcgca gtggctgcgc 60 ccgggatagc tggctgcgcc gccgcgcaca tgcctaggtt cgacgccctc ctccctttgc 120 ccaggagttc cttctgtccc ggctctgttc cgtctcgccc cgaggttcac gccatcctcg 180 gagccccagc ctttcaccca gcgcctccaa gctttggacc ttgacttctg caaaactaga 240 tggtcacagc catgaatgtc tcacatgaag taaatcagct gttccagccc tataacttcg 300 agctgtccaa ggacatgagg ccctttttcg aggagtattg ggcaacctca ttccccatag 360 ccctgatcta cctggttctc atcgctgtgg ggcagaacta catgaaggaa cgcaagggct 420 tcaacctgca agggcctctc atcctctggt ccttctgcct tgcaatcttc agtatcctgg 480 gggcagtgag gatgtggggc attatgggga ctgtgctact taccgggggc ctaaagcaaa 540 ccgtgtgctt catcaacttc atcgataatt ccacagtcaa attctggtcc tgggtctttc 600 ttctcagcaa ggtcatagaa ctcggagaca cagccttcat catcctgcgt aagcggccac 660 tcatctttat tcactggtac caccacagca cagtgctcgt gtacacaagc tttggataca 720 agaacaaagt gcctgcagga ggctggttcg tcaccatgaa ctttggtgtt catgccatca 780 tgtacaccta ctacactctg aaggctgcca acgtgaagcc ccccaagatg ctgcccatgc 840 tcatcaccag cctgcagatc ttgcagatgt ttgtaggagc catcgtcagc atcctcacgt 900 acatctggag gcaggatcag ggatgccaca ccacgatgga acacttattc tggtccttca 960 tcttgtatat gacctatttc atcctctttg cccacttctt ctgccagacc tacatcaggc 1020 ccaaggtcaa agccaagacc aagagccagt gaaggtttgg agagaacaat gaagctccag 1080 gctctctctt ctccagggca ccaagaggct gggcttagtt ttgggagaat gattaggttg 1140 ccttacctgc atggtttccc cagaggatgt gtgccccaag gtggctggaa tttttgacag 1200 acaagaaggg tgaccttggg atgggggtgt ggtctgttac tttaatgttt ctgtttttaa 1260 tgtgaaggcc aagcaggccc tgggatggga gtggggcgga ggagggtcct aagagctgat 1320 tatttaattt ctatccagaa atctttcttc ttcttgctct gtttttttaa attaaagatt 1380 tcaacaaaaa aaaaaaaaa 1399 <210> SEQ ID NO 66 <211> LENGTH: 8538 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 55009131CB1 <400> SEQUENCE: 66 ggggggcagt gaggggcgcc gcggcggcgc gcagcacggc gggaacatgg cgcgcggaac 60 cggcgcgcgc gcctagctgg cgggaccgtt agctcgaggc ggacgcggcc cgggccccgt 120 ggggatggag cagtcgccgc cgccggcgcc cgagccgacc caagggccga cccccgcaag 180 gagccgaagg cggcgggagc cagagtcgcc gccggcgtcg gcgccgattc ctctctttgg 240 tgctgacact attggccaga gaagtcctga tggaccggta ctgagcaaag ctgaatttgt 300 tgagaaagtt cgtcagagta atcaggcctg tcatgatgga gatttccaca cagctattgt 360 tctgtataat gaagccctgg ctgttgaccc tcagaactgc atcttataca gcaatagatc 420 tgcagcctac atgaaaatcc agcagtatga caaggcactg gatgatgcaa tcaaagctcg 480 acttctcaat cccaagtggc caaaggcata cttccgacag ggtgttgccc tccagtacct 540 tggacgtcat gccgatgccc tggcagcctt tgcatctgga ctggctcaag accccaagag 600 tctccagctt ctggtgggga tggtggaagc cgccatgaaa tctcccatga gagactccct 660 cgagcccact tatcagcagc ttcagaaaat gaaactggac aagagtccct ttgtggtcgt 720 gtctgtggtt gggcaggaac tcctgacagc tggccatcat ggggcctctg tggttgtctt 780 agaagccgca ctgaagattg gcacctgcag cctcaaactg agaggttctg ttttctctgc 840 cctgagcagt gcttactggt ctcttggaaa tacagagaag agcaccggat atatgcagca 900 ggacttggat gtagccaaga ccttaggtga ccagacagga gaatgccgag ctcatgggaa 960 tctgggctct gcattcttct ccaaaggaaa ttaccgggag gctctcacta accacaggca 1020 tcagttggta ctcgccatga aactcaaaga tcgagaggca gcttcatcag ccttgagcag 1080 tctgggccac gtgtacacag ccattggaga ctaccccaat gcactggcca gtcacaaaca 1140 gtgtgttctt cttgccaagc aatccaaaga tgaactttct gaagcccgag aacttggcaa 1200 catgggagct gtgtatattg ccatgggtga ctttgagaat gctgtgcagt gccatgagca 1260 gcatctgaag atagccaagg acctggggaa caagcgagaa gaggcccggg cttatagcaa 1320 cctgggcagt gcctatcact accggaggaa ctttgacaag gccatgtctt accataacta 1380 tgtcctggag ctggcacagg agttgatgga gaaggctatt gagatgcggg cctatgctgg 1440 actaggccat gctgccaggt gcatgcagga tttggagaga gctaaacaat accatgagca 1500 gcagctgggc attgctgagg atctcaagga ccgggctgca gaggggcgag catcctccaa 1560 tctaggaatc atacaccaga tgaaaggtga ttatgacact gcactgaaac tccacaagac 1620 ccacctgtgc attgcccagg agctgagtga ttatgctgcc cagggccgtg cctatgggaa 1680 tatgggcaat gcctacaatg ccctgggcat gtacgaccag gcggtcaaat accatcggca 1740 ggagctgcag atctccatgg aagtgaatga ccgcgcctca caggcctcca cacatgggaa 1800 ccttgccgtg gcctaccagg ccctgggtgc ccatgaccgg gccctgcaac actatcagaa 1860 ccacttgaac atcgcccggg agctacgaga catccagagc gaggcccggg ccctcagcaa 1920 cctgggcaat ttccactgct ctcggggaga gtatgtccag gctgccccct attatgaaca 1980 gtacctccgg cttgctcccg accttcaaga catggaagga gaagggaagg tctgccacaa 2040 tcttggctat gcccattact gccttggaaa ctatcaggag gcagtgaagt actacgaaca 2100 ggatctggca ctggctaaag accttcacga caagttgagc caagcaaaag cctactgcaa 2160 cttgggccta gcattcaagg ctctgctgaa tttcagtaaa gctgaagagt gtcagaagta 2220 cctactgtcc ctagcccagt ctctgaataa ttcccaggct aaatttcgag ccctaggaaa 2280 cctgggcgat atattcatct gtaaaaaaga tataaatggt gcaataaaat tctatgagca 2340 gcaactgggc ttagctcacc aggtaaagga cagaaggtta gaagccagtg catatgcagc 2400 cctgggcact gcataccgaa tgatccagaa gtatgacaag gccctgggtt atcacacaca 2460 ggaactggag gtatatcagg agctgagtga cttgccaggg gagtgcagag ctcatgggca 2520 cctggctgct gtctacatgg cccttgggaa atacacaatg gcattcaagt gttatgaaga 2580 gcaactggat ctagggcaaa agctgaagga tccgagtctg gaagcccagg tctatggcaa 2640 catgggcatc acaaagatga acatgaatgt gatggaagaa gccattggct actttgagca 2700 gcaattggcc atgctgcagc agctaagtgg aaatgagtct gtgctcgaca ggggccgggc 2760 ctatggcaac ctgggggatt gctacgaagc cctgggtgac tatgaggaag ctatcaaata 2820 ctatgaacaa tatttatctg tcgcgcagag tctgaatcgc atgcaagacc aagccaaggc 2880 ttaccggggc ctgggaaatg gacacagggc aatggggagc ttgcagcaag cccttgtgtg 2940 ctttgaaaag aggctcgtgg ttgctcatga acttggagag gccttcaata aagcccaggc 3000 ctatggagag ctgggaagtc tgcacagcca attagggaat tacgaacaag ccatttcctg 3060 ccttgaacgc cagctgaaca ttgctagaga tatgaaagac cgagccctgg agagtgacgc 3120 agcctgtggc ctggggggcg tttaccagca gatgggggag tatgacacag ccctgcagta 3180 ccaccagctt gatctacaga tagcagagga aaccaacaac cccacgtgcc agggccgagc 3240 ctatgggaac ctgggcctga cttatgaatc cctgggcacc ttcgagaggg ctgtggtcta 3300 tcaagaacag cacttgagca ttgctgcaca gatgaatgac ttggcggcca agacggtgtc 3360 atatagtagc cttggaagga cccatcatgc cttgcagaac tattcccaag cagtcatgta 3420 cttacaggaa ggtttaaggt tagctgagca actgggccga agagaagatg aggcaaaaat 3480 tcgccatggc cttggcctct ccctttgggc tagtggaaac ttggaggagg cccaacacca 3540 gctttatagg gcatcagcct tgtttgaaac aatccgacat gaggcacagc tgagcacgga 3600 ctacaaactc tccctctttg acctgcagac atcatcctac caggccttgc agcgggtgct 3660 cgtcagccta ggccatcatg atgaagccct ggctgtggca gaaaggggac ggacaagggc 3720 atttgctgat cttctggtgg aacgacaaac aggacaacaa gactccgacc cctactcccc 3780 agtcactatt gatcagatct tagagatggt aaatggccag aggggactag tgctttacta 3840 ttccctggct gcaggctatc tgtatagctg gctgctggct cctggggcag gaattgtgaa 3900 gtttcatgaa cactacctgg gtgagaacac agtggaaaac tcaagtgact tccaggccag 3960 cagcagtgta acccttccaa cagcaaccgg ctcagccctg gagcagcaca ttgccagtgt 4020 ccgggaggcc ctgggggtgg agtctcacta ctcaagggcc tgtgccagca gtgagacaga 4080 gagtgaagcg ggagacatca tggaccagca atttgaagag atgaacaaca aactcaactc 4140 ggtcactgac cccactggct ttctgcggat ggttcgccgc aataacctgt ttaacaggag 4200 ctgccagagc atgacgagcc tgttcagtaa cactgtgtca ccgacccagg acgggacctc 4260 ctctcttccc aggaggcaga gctcgtttgc caagcccccg ctccgtgccc tgtatgacct 4320 gctcatcgcg cccatggaag ggggcctgat gcactccagc ggccccgtgg gccggcaccg 4380 gcagctcatc ctggttctgg agggggagct ctacctcatt cctttcgccc tcctgaaggg 4440 aagctcctcc aatgagtacc tctacgagcg cttcggcctc cttgctgtcc cttccatccg 4500 ctccctcagc gtgcagtcca agtctcactt acggaagaac ccgcccacat actccagctc 4560 cacatccatg gcggctgtca tcggcaaccc caagctacca tcggccgtga tggacaggtg 4620 gctgtggggg cccatgccat cggccgagga agaggcctac atggtgtccg agctgctggg 4680 ctgccagccc ctagtgggca gtgtggccac caaggagagg gtcatgagtg ccctgaccca 4740 ggctgaatgc gtccactttg ccacccacat ctcctggaag ctgtcggcct tggtcctcac 4800 gcccagcatg gacggcaacc ctgccagcag caagagctcc ttcggccacc cctacacgat 4860 ccctgagtcc ttgcgggtgc aggacgatgc cagtgatggg gagagcatct cggactgccc 4920 gcccctgcag gagctgctgc ttactgccgc cgacgtcctg gacctgcagc tgcctgtgaa 4980 gctggtggtg cttggctcct cccaggagtc caacagcaaa gtcacagccg acggggtcat 5040 cgcgctgaca agggccttcc tggctgccgg cgctcagtgt gtcctcgtgt ctctgtggcc 5100 tgtgccagtg gctgcttcta agatgttcat ccatgccttc tactcatccc tgctgaacgg 5160 cctgaaagcc agcgccgccc tgggggaggc catgaaggtg gtgcagagca gcaaggcctt 5220 ctcgcacccc tccaactggg cagggttcat gctcatcggg agtgacgtta agctgaacag 5280 cccctcatca ctcatcggcc aggccctcac agagatcctg cagcacccgg agcgtgcgcg 5340 ggacgccctg cgagtgctgc tgcacctggt ggagaaatcc ctgcagcgca tccagaatgg 5400 gcagcgcaat gccatgtaca cgtcccagca gagtgtggag aacaaagtgg gcggcatccc 5460 tggctggcag gccctcctca ccgctgtggg cttccggctg gaccccccaa ccagtggcct 5520 gccagcggct gtcttcttcc caacctccga cccgggcgac cggctccagc agtgcagcag 5580 cacactccag tccctgctgg gtctgcccaa tcctgccctc caagcccttt gcaaactcat 5640 cactgcctcc gagacgggcg agcagctcat cagccgggct gttaaaaata tggttggaat 5700 gctccaccag gtgctggttc agctccaggc tggcgagaag gagcaggact tggcatcagc 5760 tcccattcag gtctccatca gcgtccagct gtggcggctc ccgggatgcc acgagttcct 5820 ggcagctcta ggttttgatc tctgtgaagt tggtcaggag gaagtaatcc tgaaaaccgg 5880 gaagcaagct aatcgacgga ctgtgcactt cgcgctccag tccctgctgt ctctgtttga 5940 ttctactgag ctacccaagc gcctcagcct tgacagctcc tcctccctcg agtctcttgc 6000 ttctgctcag tctgtttcca acgccctgcc cttgggttac cagcaacccc ccttctctcc 6060 caccggtgcg gacagcatcg cctcagatgc catctctgtg tacagtctga gctccattgc 6120 ctcctcaatg agctttgtct ccaaacccga gggtggatca gagggtggag gccccggagg 6180 acggcaggac catgaccggt ccaagaacgc ttacctgcag agatccaccc tgcctaggag 6240 ccagctgcct ccccagaccc gccctgcagg caacaaagat gaagaagaat atgaagggtt 6300 ttctatcatc agtaacgagc ccttggcgac ctaccaagaa aaccgaaaca catgcttctc 6360 accagaccac aaacaacccc aacctgggac agccggaggc atgagagtct cggtgagctc 6420 caaagggagc atcagcactc caaattctcc agtgaaaatg actctgattc ccagccccaa 6480 ctcacccttc caaaaggtgg gaaaactagc aagctcagat acaggagaat cagaccagtc 6540 tagcacagaa acggacagta ccgtgaaatc ccaagaagaa agcaacccaa aactggatcc 6600 acaagagtta gcccagaaaa ttctggagga gacacagagt catctcattg cggtggagcg 6660 tcttcagagg agcggcggcc aggtgagcaa gagtaataac cctgaagacg gcgttcaggc 6720 gcccagcagc actgctgtct tcagagcgtc agaaaccagt gcgttcagca ggcctgttct 6780 ctcccatcag aagagtcagc catcaccagt cactgttaaa ccaaagcccc cagccaggag 6840 ctcctccctg cccaaggtga gttccggata tagcagcccc accacctcag agatgtccat 6900 caaagacagc ccgagccagc acagtggccg gccatcgccc ggctgcgact cacagacttc 6960 ccagctggac cagcctctct ttaaactgaa gtaccccagc tctccttaca gcgctcacat 7020 ttccaaatca ccaaggaaca tgtccccaag ctccggccac cagtctcctg ctggcagtgc 7080 accctcccca gctctctcct actcctcagc tggatctgct cgctcaagtc cagcagacgc 7140 tcccgacata gacaaactga aaatggcagc cattgatgaa aaggtgcagg ctgtccataa 7200 cctgaagatg ttctggcaga gcacacccca gcattccaca gggccaatga agatcttccg 7260 gggggctcct ggcacgatga cttccaaaag ggatgtcctc agtctgttga atttgtcacc 7320 acggcacaat aagaaggagg agggagtgga taagcttgaa ctgaaggagc tgtccctgca 7380 gcagcatgac ggagctccac cgaaagcccc tcccaacgga cactggcgca ccgagaccac 7440 ctcgctgggc tcactgccgc tgcccgccgg ccctcccgcc acagcccccg cgcgcccttt 7500 gaggcttcct tctggaaatg gctacaagtt cctgtctcca ggaagatttt tcccttcttc 7560 caaatgctaa agcatctttt atacccactg actctgagca gcctgcagat gggggcctgg 7620 cgtttgcttc agcccttccc tgagtgcagt ccccccacag ccaccagcac cctcatgatg 7680 ctgtgctctg caggcgaggg gcaccaccac gtccaaaggc tgccacacac actggtggct 7740 tttctgggcc acattcacca aaagccagga cttctgtggg gctggtacag gaggctcatg 7800 gaatttccta cacacttcac caaatgtttg tttacctttg aactccctgc ttctcatctt 7860 tgatatgatt cttcaccagg attttgtaca aaaatgatca tggttctggg gtggggagag 7920 gaaagggagc acatattttg ctaagaggta tatatgcagt accttttata cacagaaata 7980 caaatagagc tttttctaag gctttcggtt gctggttggg ggtgggatat atgaaatttc 8040 agttgaattc tacaggaaag tgttatatta gccaaaaaca gaaaaatggt ttttaaaatg 8100 ccaatgattt gtaattaaat tgtagcaatt ttggtctcat gatagtgtaa tatctcagca 8160 acaatgcaat aattcacatt gaaacagcgc ttccattctg aactctgctc tgcaaatgtc 8220 ttttgggtcc cgctgtcaac caaacttgaa ttttcttaaa aaaaaaatta tgtaactctt 8280 atccaggcat tttagaacta tgcaattgtg atttaaaatg caactttgtg cttttaaaac 8340 attattgacc ttttttgtat atggataaac aacttggttt tattatcaat agtactttgc 8400 atttatagct attattttta aaagctcaaa aagtttttta aaatgtcaaa ttttgaatag 8460 tcatcaataa gtaattatca agtttggaag gaaaggttga aatgactccg tttccttata 8520 agcaaaaaaa aaaaaaaa 8538 <210> SEQ ID NO 67 <211> LENGTH: 545 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1538253CB1 <400> SEQUENCE: 67 cttaaacggc cgcccctttt tttttttttt gaggtagggt ctggttctat cacccaggct 60 ggagtgcaag tggtaccatc atggctcact gcagccttga cctctcaggc ttgagtgatc 120 ctcccgcctc agcctcccaa gcacctgggt ctacaggtgt ccaacaccat gtacagctaa 180 tttttaaaat ttttgtagag atggagtctc actttgttgt ccaggctgtt ctcacactcc 240 tgggcttaag taattcttct gccttggcct cccaaagtgt tgggattaca ggcgaaagcc 300 actgcaccag gccatgagga gtcttccatt cactttttac ttctattcaa cgtcctgagt 360 aaagcaggga tcacgggggg cctccttccc atctgctttg atagaggaag caagacttct 420 gggccggcac taggagctgg cacgagcatg tctcagcccc cacttactcc tgtgtgtgta 480 tcccataaaa ggctggccgg ccgcctttgt ctacgtcgct cataggaagg tgagtcccct 540 ttgac 545 <210> SEQ ID NO 68 <211> LENGTH: 1297 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 030658CB1 <400> SEQUENCE: 68 ccgccgccac tgccgggaga gctcgatggg cttctcctgc gcgccgcccg gtgtctggcc 60 gagtccagag agccgcggcg cctcgttccg aggagccatc gccgaagccc gaggccgggt 120 cccgggttgg ggactgcagg ggaaggcagc ggcggcggcg gcgggagccc caccggggtc 180 tgggactggg gaactgcctc cggcttcacg atgccagtat ggacagaata gcttatgatg 240 cttatcccca cccaccactt ccgaaacatt gagcggaaac cagaatacct ccagccagag 300 aagtgtgtcc caccccccta ccctggtcct gtgggaacca tgtggtttat ccgtgacggc 360 tgtggcatcg cctgtgccat cgttacctgg tttctggtcc tctatgcgga gttcgtggtc 420 ctctttgtca tgctgattcc atctcgagac tacgtgtata gcatcatcaa cggaattgtg 480 ttcaacctgc tggccttctt ggccctggcc tcccactgcc gggccatgct gacggacccc 540 ggggcagtgc ccaaaggaaa tgccactaaa gaattcatcg agagtttaca gttgaagcct 600 gggcaggtgg tgtacaagtg ccccaaatgc tgcagcatca agcccgaccg agcccaccac 660 tgcagtgttt gtaagcggtg cattcggaag atggaccacc actgtccctg ggtcaacaac 720 tgtgtaggcg agaacaacca gaagtacttc gtcctgttta caatgtacat agctctcatt 780 tccttgcacg ccctcatcat ggtgggattc cacttcctgc attgctttga agaagattgg 840 acaaagtgca gctccttctc tccacccacc acagtgattc tccttatcct gctgtgcttt 900 gagggcctgc tcttcctcat tttcacatca gtgatgtttg ggacccaggt gcactccatc 960 tgcacagatg agacgggaat agaacaattg aaaaaggaag agagaagatg ggctaaaaaa 1020 acaaaatgga tgaacatgaa agccgttttt ggccacccct tctctctagg ctgggccagc 1080 ccctttgcca cgccagacca agggaaggca gacccgtacc agtatgtggt ctgaaggacc 1140 ccgaccggca tggccactca gacacaagtc cacaccacag cactaccgtc ccatccgttc 1200 tcatgaatgt ttaaatcgaa aaagcaaaac aactactctt aaaacttttt ttatgtctca 1260 agtaaaatgg ctgagcattg cagagaaaaa aaaaaaa 1297 <210> SEQ ID NO 69 <211> LENGTH: 732 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7486348CB1 <400> SEQUENCE: 69 atggcatgct ggtggccgct cctgctagag ctgtggacag tcatgcccac ctgggctggg 60 gacgagctgc tcaacatctg catgaatgcc aaacaccaca agagagtgcc cagcccagaa 120 gacaagctct atgaggagtg catcccctgg aaggacaatg cctgctgcac cctcacgaca 180 agctgggaag cccatctgga tgtatcccca ctctacaact tcagcctgtt tcactgtgga 240 ctgctgatgc ctggctgtcg gaagcacttc atccaggcta tctgcttcta tgagtgctcc 300 ccaaacctgg ggccctggat ccagccagtg gccccgagtg ggcagggaga gcgagttgtg 360 aatgtgccgc tgtgccagga ggactgtgag gagtggtggg aagactgtcg catgtcttac 420 acatgcaaat ccaactggcg tggtggctgg gactggagtc aggggaagaa ccgctgcccc 480 aaaggggccc agtgcctccc tttctcccat tacttcccca ccccagctga cctgtgtgag 540 aagacttgga gcaattcctt caaagccagc cctgagcgac ggaacagtgg gcggtgtctc 600 cagaagtggt ttgagcctgc tcagggcaac cccaatgtgg ccgtggcccg cctcttcgcc 660 agctctgccc catcctggga actgtcctac accatcatgg tctgctccct gttcctgccg 720 ttcctttcct ga 732 <210> SEQ ID NO 70 <211> LENGTH: 540 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3359663CB1 <400> SEQUENCE: 70 cccacgcgtc cgcgcactag accgcggggt agtcggcgcg aggcggagct tggcagttcc 60 gtccacttca gccgcagcgt ccctcgccgg gtgtctcgcc gcagcctccg gagaggaaca 120 gaccctcact ctctctgtca gaaaaatgtc tgctccagct cagccacctg ctgaagggac 180 agaagggact gccccaggtg ggggtccccc tggccctcct cctaacatga ccagtaacag 240 acgactacag caaacccagg cacaagtgga ggaggtggtg gacatcatac gtgtgaacgt 300 ggacaaggtc ctggagaggg accagaagct gtcagagctg gatgaccgag ctgatgcctt 360 gcaggcagga gcatcacaat ttgagagcag tgctgccaag ctaaagagga agtattggtg 420 gaaaaactgc aagatgatga tcatgctggg agccatcttt gccatcatcg tggtagttat 480 tgtaagtaag tatcgctgaa gttgctggtg ggataagagg tgggaaggtc ctggagtctt 540 <210> SEQ ID NO 71 <211> LENGTH: 1535 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3237418CB1 <220> FEATURE: <221> NAME/KEY: unsure <222> LOCATION: 1482 <223> OTHER INFORMATION: a, t, c, g, or other <400> SEQUENCE: 71 gaattcggcg cgggctgcag acggctgcga ggcgctgggc acaggtgtcc tgatggcaaa 60 tttcaagggc cacgcgcttc cagggagttt cttcctgatc attgggctgt gttggtcagt 120 gaagtacccg ctgaagtact ttagccacac gcggaagaac agcccactac attactatca 180 gcgtctcgag atcgtcgaag ccgcaattag gactttgttt tccgtcactg ggatcctggc 240 agagcagttt gttccggatg ggccccacct gcacctctac catgagaacc actggataaa 300 gttaatgaat tggcagcaca gcaccatgta cctattcttt gcagtctcag gaattgttga 360 catgctcacc tatctggtca gccacgttcc cttgggggtg gacagactgg ttatggctgt 420 ggcagtattc atggaaggtt tcctcttcta ctaccacgtc cacaaccggc ctccgctgga 480 ccagcacatc cactcactcc tgctgtatgc tctgttcgga gggtgtgtta gtatctccct 540 agaggtgatc ttccgggacc acattgtgct ggaacttttc cgaaccagtc tcatcattct 600 tcagggaacc tggttctggc agattgggtt tgtgctgttc ccaccttttg gaacacccga 660 atgggaccag aaggatgatg ccaacctcat gttcatcacc atgtgcttct gctggcacta 720 cctggctgcc ctcagcattg tggccgtcaa ctattctctt gtttactgcc ttttgactcg 780 gatgaagaga cacggaaggg gagaaatcat tggaattcag aagctgaatt cagatgacac 840 ttaccagacc gccctcttga gtggctcaga tgaggaatga gccgagatgc ggagggcgca 900 gatgtcccac tgcacagctg gaatgaatgg agttcatccc ctccacctga atgcctgctg 960 tggtctgatc ttaagggtct atatatttgc acctcctcat tcaacacagg gctggaggtt 1020 ctacaacagg aaatcaggcc tacagcatcc tgtgtatctt gcagttggga tttttaaaca 1080 tactataaag tctgtgttgg tatagtaccc ttcataagga aaaatgaagt aatgcctata 1140 agtagcaggc ctttgtgcct cagtgtcaag agaaatcaag agatgctaaa agctttacaa 1200 tggaagtggc ctcatggatg aatccggggt atgagcccag gagaacgtgc tgcttttggt 1260 aacttatccc tttttctctt aagaaagcag gtactttctt attagaaata tgttagaatg 1320 tgtaagcaaa cgacagtgcc tttagaatta caattctaac ttacatattt tttgaaagta 1380 aaataattca caagctttgg tattttaaaa ttattgttaa acatatcata actaatcata 1440 ccagggtact gcaataccac tgtttataag tgacaaaatt anggcaaagg tggttttttt 1500 ttaaatcaag gagcttgtta ctggctctac tgaga 1535 <210> SEQ ID NO 72 <211> LENGTH: 3768 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2529616CB1 <400> SEQUENCE: 72 tttttttttt gaataatata acagttttat tataaatcaa aacaccaaac ttttgcaaac 60 tttacataaa cgtgtagcca tatgactgta taacaagagc ccaagagcaa ccattgtcta 120 acaggtagaa atgcagacag tttcatgtta agcctttaga atttcctttc acggcaggtt 180 tccaaaataa actaactttt ctaacattta ttctcacaaa aatatatttc aagttagaat 240 aaacaactca ttggcttcag acatttaatt gtatgtattt aaccatactc agataattgt 300 catatttagc caaatggagg ctttttctgt gacctatttc caaattctca gattctggtt 360 catctactcc ttcaagcagt ttggaatgac ttgccagttg gcatttatat cattggaact 420 attctgcaaa taagccattt tgataaagct tgcttggttt gagacaacta tgtatttgga 480 gataaaagac tcagaacaaa gtgcttgcct tttctacagt ttatatcaaa cgagatgggc 540 acttaagcag tcagcctgga ttcatatgtc tagagtggcc aggctgtaaa tacaataagt 600 ctagctgcct tccacatgtg gtcagacagc tatattaaga agatctactc actgctggtt 660 atgaagatag ccaggagctt gtctgattta aggaactatt cagccattga aggatagaca 720 ctcccaaaaa tggaatttca gggaagtgta gaatgaacaa tcctgttcaa agcagccaaa 780 attattttct gcatgccaag atgttattca cacacataaa tactatatgc agataatctt 840 catttttgaa ttacaagttg ttttattgca aaagcaagta tagttataat atatagcaaa 900 gcgaatctat ctttggttct atatagcaga taattttttt gcaaaaataa ataggcatgg 960 caagaaaaat acttcaacta tcttaaggga aaacccaata ttttataaaa attaagcaag 1020 gaatatagaa atgatgtatc tttcagactt ttttccaatc atcttcgtta atatctaaca 1080 ccagtgcaat tttaacatta aaataattgt gcacaatata tttaacaata cagcatagac 1140 tcaaaagtgt cataaaacaa aatagtactt tcccttcaaa atcatttagg aattatgctt 1200 tctaaaaaat gtacgggaaa gtagaactgc tgaaatatgt tgacaaaatt aactttgaag 1260 aagcgcaaga aaaggaaata aagatgtaat tataaccaca gatcctagag atctcaaaaa 1320 aagtgaacac attatccatg ctcccatttg cagaaaatat gtattagaga gaattgttca 1380 gagacttttt tcaactagta tctatgagag ctccctgtca tggtttcaac tttcagcaca 1440 tttagtgagc ttcatttgtt ggtgcttttc gtctcttttc atatattatt tttgcatcaa 1500 ataattctct ttccctgtag cctagacatg gtccttttag atactttgct tcagctgcct 1560 cgtaatctaa cccatcaaca gcagaaattg aacaaataat tgcttctggc agaagaactt 1620 ctaggataaa tttaatttta tcatctttta tccaagttgg cattatttga tctatttgat 1680 tgcagacttc ttgtaaatat ttcaccactt catccaactg atcttcatcc tcaaagtatg 1740 tttcaataca gggtgtgaac ctatttgcat tcaaaaatga tttcagccat ctggatcctt 1800 ttgtgccatt tacaatggcc agaagatggt tctctgttcc ctttgcattc acaatgaagt 1860 ccaccaggtt cttgttggct cggtcccgag cagccttcat ccggtcaggg agaatttttt 1920 ggaaggacat tttcttggtc tgggaagtta cagccatcgg ttccctggca tcttcattat 1980 gcagctttgg aaatttgttc ctgaaagtat cctgttttgt ttctttccta actgggtaac 2040 taatatcagc agcataatac tcaagcaaag agcccgtgaa agaaccacaa cctattctaa 2100 ctctgtagtc acaaattagt gagatgcacc agtcaatact ctcactataa tcctccctgg 2160 ctttgtccac tagcatttgt ttctctttac aatcaaattt ctttaatctt ctaaaattta 2220 ctctaatgcc cttcttttca gaattcatgt ttgcctcaac aaaaagcaca cttgctttcc 2280 tctcttttcg tctgatactt tttatcactg ctggccaaaa tggatatttc tgatatttaa 2340 accagactat cattcctgtt tcaaacggat gtgtctcata atgtaaaatg aagcgtggaa 2400 gttcttcgtc ttcctcatca tcatctaata gagaaagatt aatgcgactt ggaagcaatg 2460 acttgtcaga ggcttgacct tcttcctcaa gttcttcaaa atccagtctc tgaaaatttc 2520 tttcactact cataagatgt gaataatccc agacagggtt agaggcacta aatgaaacct 2580 cgcattccct tgaacaactc ccagggcatg ctgcagcccc catctctgat tccatggaag 2640 gttgattctg gctggtatct aagcatggat ttgagggacc ctctccagga tcctcaatat 2700 tctctgagaa agcagagcat tcagagggaa cagccagggt ctctaggcag gtatcctcgc 2760 tctcttcttt caaagctttg ggcataatga gcatatctga tgacaaaggt gacaaaggtg 2820 gagcaaactt ttcatcttta acacatgcac tttcctcttt gactgcagaa tgcacagaca 2880 taactgctga gatatcaatc ttattcttgt tctctttttc atcattatct tccgaaagtg 2940 aagggaaagt ctcgcaccag ctagagtttt gtaatgactt tgtttccact tcacttggaa 3000 tagtatcgac cattgtgggt gcttgtgatt tatcatcata cagggaatca tcactctctg 3060 aagatgctaa caagcatgct gagttttccc tttcctcaag acaccctggt aagtcacctt 3120 catccttccg gtatttttta tgagggggtg aatcggactg tttttgtggt acattttgag 3180 acagcatagt gatctcctct tcatctgaag tgcttgcttg actcaaattt gttctctcat 3240 tcagaatacc cagtgccact tttagtgatc ttccataggc agtttcctct gtaggtggag 3300 cactgtcctc tgactgtagt cctaatgagg cagcaatggc ttcaatttga gatttattta 3360 ggatctttgt ttctgtgctg tccaatttaa ttttttcatc tagtgagagt atttgaactt 3420 ctagagaaaa tgcctttttc ctcttactgt ttgatgaagt ttcagatctg gacaaaactt 3480 ttgctggcca caactggtct ttccagttgc ataggacata ctcagactcc attatggttt 3540 atatttgtgt gccaagggtt attaccaaag gttgaggtgg ctatctttgt cactgctaat 3600 gcaagttcta cccaaaacaa tactcttaac aaatcctctt tcgtcttatg actacaaagg 3660 gtttacagct tgtgtggcct gttctccacc tcaattttcc aaggatgctt gaacacgttg 3720 tttgaatagg atgataccgg aagataccac tgtcatgtgg atcctggt 3768 <210> SEQ ID NO 73 <211> LENGTH: 2573 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7475662CB1 <400> SEQUENCE: 73 atgaggaccc agagccttct cctcctgggg gccctcctgg ctgtggggag tcagctgcct 60 gctgtctttg gcaggaagaa gggagggagc acaccccaat attcagccca gctgctcaga 120 ggcaaagagc tggcacagca gaaaccgagc ctgcgcaggg ccactctgca tgggcagagg 180 aacgcctcag agacagagtt aacgcctgat cctcgaaacc atgccatttg caacagtgat 240 gaacgcaacg gtgcagaaga cgtggccagc tgtggctgtg acagtgcacc aggctggcca 300 ctgctgacgc acgaaggagg tggcaaattc cctgctctat ctgctgggcc tcttgtgtcc 360 agcacaagac tgagggactg ggcggtccac tgtggaggta cacttgggaa tccttggtct 420 tctttccctg ttctcttgac cttgcagtat gatgacagag cttctgccct ctgccatgag 480 aagagcttgc ccggagccac ttgtcttgct ggagagacac ctggggcaag cctgaagctg 540 agccagacca gccaagcctc aaacttgcca aagagaaaaa aatatttgtg gaaaaatggc 600 tataggagta cagaagttca ccaggaagag aagaagccag tacttcaggt tctccctgtg 660 cggagccata gcaggctctg gcagcctcag gaaagcccca gataccagct gtcaggagga 720 aaaacatacc aggagcctgt gtgcacaaaa gcggtaaagg atcccagagg agctgtgggc 780 acgaatgagt cacataagaa tggtggagga ggaagtgaca aggagcctgg gtcttcaggg 840 ctattcatga gcagctgtac ctaccctggc ctgccaaaaa aaaaaaaata tgatgctacc 900 cggttccaca gacagggaaa caagcccaga gagggcgacg aatgcactca aggacagcag 960 ctagtgatgc tgatgctgct ggtccgggga acacactatg agaacctccg gtctaaagtg 1020 gtgctgccaa cacccctagg agggaggagc actgaaacct ttgtgagcga gttcccgggc 1080 cccgacaccg ggatccgctg gcggcgaagc gacgaggcgc tgcgcgtgaa cgtgggtggc 1140 gtgcggcggc agctgagcgc gcgcgccctg gcgcgcttcc cgggcacgcg gctgggccgc 1200 ctgcaggccg cggcgtcgga ggagcaggcg cggcgcctgt gcgacgacta cgacgaggcg 1260 gcgcgcgaat tctacttcga ccggcacccc ggcttcttct tgagcgtgct gcacttctac 1320 cgcactggcc acctgcacgt gctcgacgag ctgtgcgtct tcgcctttgg ccaggaggcc 1380 gactactggg gcctaggcga gaacgcgctt gccgcgtgct gccgcgcgcg ctacctggag 1440 aggcggctga cccagccgca cgcctgggac gaggacagcg acacgccgag cagcgtggac 1500 ccgtgccccg acgagatctc cgacgtgcag cgagaactgg cgcgctatgg cgcggcgcgc 1560 tgtggccgcc tgcgccgccg cctctggctg accatggaga acccgggcta ctcgctgccg 1620 agcaagctct tcagctgcgt ctccatcagc gtggtgctcg cctccatcgc cgccatgtgc 1680 atccacagcc tgcccgagta ccaggcccgc gaggcggcgg ccgccgtggc tgcggtggcc 1740 gcgggccgca gcccggaagg cgtgcgcgac gacccggtgc tgcgacgcct cgagtacttc 1800 tgcatcgcct ggttcagctt cgaggtgtcg tcgcgcctcc tgctggcgcc cagtacgcgc 1860 aacttcttct gccacccgct caacctcatc gacattgtgt ctgtgctgcc cttctatctc 1920 acgctgctgg ctggtgtggc actgggcgac cagggcggca aggagttcgg ccacctgggc 1980 aaggtggtgc aggtgttccg cctcatgcgc atcttccgcg tactcaagtt ggcgcgccat 2040 tccaccgggc tgcgctcgct gggagccacg ctcaagcaca gctaccgtga ggtgggcatc 2100 ttgctgctgt acctggctgt gggtgtgtca gtgttctctg gtgtggccta cacagctgaa 2160 aaggaggagg acgtgggctt taacaccatc ccagcctgct ggtggtgggg cacagtgagc 2220 atgaccaccg tgggctatgg ggatgtggtg ccagtgacgg tggctggcaa gctggcagcc 2280 tcaggctgca tcctaggggg catcctggtg gtagcactcc ccatcaccat catcttcaac 2340 aagttctccc acttctaccg gcgccagaag gctctggagg cagccgtgcg caacagcaac 2400 caccaagagt ttgaggactt gctgagcagc attgatgggg tgtcggaggc atctctggag 2460 acatcccgag aaacctctca ggagggacag tctgcagatc tagagagcca ggcccccagt 2520 gagcctccac accctcagat gtattaaaac caggtatccg tgaccccctg cca 2573 <210> SEQ ID NO 74 <211> LENGTH: 1111 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 3811024CB1 <400> SEQUENCE: 74 ctgaagagga gctcacagtt cccagcgtct gctcccacgg tgtccagcgc ccagaatgcg 60 gcttctggtc ctgctatggg gttgcctgct gctcccaggt tatgaagccc tggagggccc 120 agaggaaatc agcgggttcg aaggggacac tgtgtccctg cagtgcacct acagggaaga 180 gctgagggac caccggaagt actggtgcag gaagggtggg atcctcttct ctcgctgctc 240 tggcaccatc tatgcagaag aagaaggcca ggagacaatg aagggcaggg tgtccatccg 300 tgacagccgc caggagctct cgctcattgt gaccctgtgg aacctcaccc tgcaagacgc 360 tggggagtac tggtgtgggg tcgaaaaacg gggccccgat gagtctttac tgatctctct 420 gttcgtcttt ccagcttctc ctgggctcta cccggcagcc accacagcca agcaggggaa 480 gacaggggct gaggcccctc cattgccagg gacttcccag tacgggcacg aaaggacttc 540 tcagtacaca ggaacctctc ctcacccagc gacctctcct cctgcaggga gctcccgccc 600 ccccatgcag ctggactcca cctcagcaga ggacaccagt ccagctctca gcagtggcag 660 ctctaagccc agggtgtcca tcccgatggt ccgcatactg gccccagtcc tggtgctgct 720 gagccttctg tcagccgcag gcctgatcgc cttctgcagc cacctgctcc tgtggagaaa 780 ggaagctcaa caggccacgg agacacagag gaacgagaag ttctgcctct cacgcttgaa 840 ctccctgatg ttttctctga gcctgccttg gctctgagac caaggtggtg tggctgctct 900 gggacccagg ctgagggtgg tgctctgggg accaggggca agagaataag ggtccctgtg 960 cccattgtct ggagctggga acctgcccca aggctactgc tgcaagaaga gactgtgccc 1020 tccgaggcca gcactccaac ggagggggct gcagcatcgc acttcaggca acagaagccc 1080 ctcctggtca acctcctccc tctgctgttt a 1111 <210> SEQ ID NO 75 <211> LENGTH: 1396 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1683407CB1 <400> SEQUENCE: 75 gccctgccgc gcgcgcatgt aggcgttccg agcggcggcg gaggtgagcg cacggacgag 60 cgggagggac ccttctccgg cctgatgcga cccgattgtc cgcagtgact acactcatgg 120 caggtcccct gtggcggacc gcagcatttg tgcagagaca caggacaggc ctcttggtgg 180 gttcctgtgc aggcctgttt ggagttccag tctcgtacca cctcttcccg gatcccgtgg 240 tccaatggct ctaccagtac tggcctcagg gccagccagc tccgctccct ccacagctgc 300 agagcctctt ccaagaggtg ctacaggaca taggtgttcc ttcaggccat tgctacaagc 360 ccttcaccac cttcaccttc cagcctgtga gtgcaggctt cccaagactc cctgctgggg 420 ctgtggtggg catccctgcc agtttcttgg gagacctagt gatcaacact aaccatcccg 480 tggtcataca tgggcataca gtggactggc ggagcccagc aggcgcccgg ctgagagctt 540 ccctgacctt gtcccgtgaa gcccagaagt tcgccttggc cagggaagtg gtgtacctgg 600 aaagcagtac cactgccgtg cacgccctgc tggccccagc ttgcctggca gggacctggg 660 cactgggcgt gggtgccaag tacaccctgg ggctccatgc aggccccatg aatttacggg 720 ctgccttcag cttggtggca gcagtggcag gctttgtggc ctacgccttc tcccaggatt 780 ctctcactca tgccgtggag tcctggctgg accgccgcac ggcctccctc tctgcagcct 840 atgcctgtgg tggagtggag ttctatgaga agcttctgtc gggcaacctg gccctgcgca 900 gtctcttggg caaagagggg gagaagctgt atacacccag cgggaacatc gtccccagac 960 acttgttccg aatcaaacat ttaccctaca ccacccgccg ggactctgtg ctgcagatgt 1020 ggagggggat gctcaatccg ggccgctcct gatgggctca tcacaaggac acttccagct 1080 tgtgcagaca ccaccctgcc attgagtctg gagggccctg ttggagcctt tggacctata 1140 gctcaaggcc agaaaaatca ctggctttgg aattaaatag cttagattgt actataacca 1200 ctacttatga actcagggac tatgagggac tattcagggg ctatgaatct gagcctttgt 1260 ttcttgaact gtaaagtgga gatgatgtaa accgccttgc aagattgtag agttgggtaa 1320 ggtcatgaac ataagggcct ggcacaaagg gtgcactgta aataaacaga catccctcct 1380 taaaaaaaaa aaaaaa 1396 <210> SEQ ID NO 76 <211> LENGTH: 1465 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1319969CB1 <400> SEQUENCE: 76 caggtttagg acaaagaagt gtgttgcaac tgaggtaaaa ggtctttaaa aagcatatta 60 gctgactata tggatgttct tcagttcaaa cctgaccacc ctttgctctc acatggaaat 120 acatccacta gcagtgttgt aagtgatcct atcagcaaac gtgtgcatca gtgctcctcc 180 agaacatcat atttacgtta gggcttaata ggacattcat aaagcaacat gcagtttgtt 240 atttttaaat gcatgtgacc tccttatttc aaaagcaagt atctttaaac atagtaatag 300 catttctcta tatgcaaacc tctgtacatg aaaaggttta cattttaaaa caaacatgtt 360 tttgagtttt atccaaattc aaaaaaggca tctgaaaaat ttaacagctg aaaaacactt 420 tctccttgct gggaaaactt aaaccttgct aggctttatg caacttaaaa aaaaaaaatc 480 acttctgtgc tgagaactag catgagaaat ctcagcatga aaggttggtg gatttttttt 540 cttcataaaa ctaagcccaa ttgttggttt taagagtgat gccacaatat acatatgctt 600 tgttaggaac aaatataatc taatttcaag ggcatcttca acaaaaatta gggggaaaag 660 ataaaggcta cttaagcagt gatccagtgt ctgaaagcaa aggttgagaa catcattgta 720 ccatcaaggt ctagaaatgc tgctaaccct gagcgggttg ttactgtttg aaaagcctat 780 gggtatttgt tttattgttg tctcactcaa ttcttactta gctgagagta tctcacaagg 840 gaagtactgc tctgtgatgg tgtcctggac tttgttttct atttgtttca gcacttcaat 900 aaatggtctg ttacctgcca ttatgacctg tatgcatttg ctgagcagtt tttcaaaaca 960 aaacaaatta tgtggctgta tttctagaac gctgagccat tttcaagata gtatagaatt 1020 agaaacacac atagacacgt ccacacaatt gtatgtttat actgaacaca tatattcaga 1080 catattcagg aaaaaaaaaa aaaagaaaat aggttggaca atacaaatat ggaaatacag 1140 cttgttcaat catttagagc ccatacttct aacggtgtac atatgtagac gtgactttgt 1200 aaagaagacc cacatgtgtg tctacactca agcatcttcc tcttaatact ctactgagga 1260 taaaggacac aaagtaattt ttgaaatatc atgctggcta cttttagagt atattagtgt 1320 gagtagtgac ttaagaggtc aggtttaaga gaagtagcaa catacttcta ttatttacat 1380 ggtgattttt tttttataag tccttccttg aaggcagact tagatatttc aagacctcct 1440 tagaaaaatt tttcagcacc ttctg 1465 <210> SEQ ID NO 77 <211> LENGTH: 2100 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1645034CB1 <400> SEQUENCE: 77 ggcagccagg ccgcagctgt ggactcctca cctcccggag gctctgctgg tgcaggcccc 60 gcattggagg gctcgattgg ctgcccggct ggcactgacg tccccttgga gctgggtggc 120 agaggagata aacagccatg tgcaactctc cacactatat ttaacagctg cggcggagaa 180 ggcagggagg cagccacggt ggcggctctg ggggcagctc ttgtcttcgg ggagaaggcc 240 cttggagccg ggctggcatc ggccttctcg gggtgagcga ggtcaccatg ccagcttccc 300 agagccgggc ccgtgcccgg gaccgcaaca acgtcctcaa ccgggctgag ttcctgtccc 360 tgaaccagcc ccccaagggg ggcccggagc cccgcagctc gggcagaaag gcctcgggcc 420 catcagcaca gcccccacct gctggtgacg gggccagaga gcgacgccag tcacagcagc 480 tgccagagga ggactgcatg cagctgaacc cctccttcaa gggcatcgcc ttcaactccc 540 tgctggccat cgatatctgt atgtccaagc ggctgggggt gtgcgctggc cgggcggcgt 600 cctgggccag tgcccgctcc atggtcaagc tcatcggcat cacgggccac ggcatcccct 660 ggatcggagg caccatcctc tgcctggtga agagcagcac actggccggc caggaggtgc 720 tcatgaatct gctcctggcc ctgctcctgg acatcatgac ggtggccggc gtgcagaagc 780 tcatcaagcg gcgcggcccg tacgagatga gccccagcct cctggactac ctcaccatgg 840 acatctacgc cttcccggcc gggcacgcca gccgcgccgc catggtgtcc aagttcttcc 900 tcagccacct ggtgctggcg gtgcccctgc gcgtgctgct ggtgctctgg gccctctgcg 960 tgggcctgtc ccgcgtgatg atcggccgcc accacgtcac ggacgtcctc tccggctttg 1020 tcatcggcta cctccagttc cgtctggtgg agctggtctg gatgccctcc agcacctgcc 1080 agatgctcat ctctgcctgg tgaagcgccc gccggcccac acaagcctct gggggcaggg 1140 ctggccctag agaaggggca gggggtggcg aggtggcggg cgtgggtgga acagagcggc 1200 caggagtcag agcggccacc cccacctcat cttcccctcc tggctggagg ctggcgaacc 1260 caggccaccc ctcccggaga caagcgtgtt tggcagtgcc aggcctcttg cccctttgct 1320 tggactccaa gtctcctctc tgggcagcca ggacccaccc atggggacag ccctatttag 1380 cttctgctct gggaacagca aaaatcagga tggtgggagg ggccgagtct tgtcttgtcc 1440 tttcatcatc atgactgttg agttcttggc tgtgcccatc acgccacagc acgacgcctg 1500 ccaaaatgcc cccaacctac tgcctgatgc aggtgccatt gccattagcg gtcatcgaca 1560 gcttagggca gcactttcca acgggtgccc atgggacacc agcctgcgag atgcttttgt 1620 gggaaagggg ttttgtggtt caataacttt cggaagtgct gcacactctg tccccaagtt 1680 ggacattcac aaaggccgtt attgccgtaa aggctctgac aagccctata gaaaagcttc 1740 ttgctaaacc ttctttaacc catgttttct aaacttattt gaccacagaa cccttttctt 1800 ggggaacagc tattaacccc caaggaatta ttggttcctc aagtgcgttt tgggagctgc 1860 tgccagagag ctaaagggcc tggggtgtga gctgactctc cgctggggag gccgggtgca 1920 cacgccacag cccgaggaaa gtgctggcca ccgcccgtgg gcatcgatga ggctttggcc 1980 cccaggggcc ggactccgtg tgacctaata ggtcgtttcc aagtcacccg ttttggatgt 2040 gcatttcatg tgacaataca gatgacatgc aaatggccca aaaaaaaaaa aaaaaaaaaa 2100 <210> SEQ ID NO 78 7<211> LENGTH: 1823 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7949783CB1 <400> SEQUENCE: 78 tttcgggaag gatcgcgcaa gggttaatga tgaaagctgg cgaccaggtg gggcgcccac 60 acccgccccc ggccacggtg ggcgtcggag gtgagggggc gctattcggg cagcagtgct 120 ccgggtggcg cgcgggagag ctgccaggct gacggagagg ccggcccgag tgggggccgc 180 tccgccgccg ccgccgccgc cgccgctgtg atgcggagcc ggtgctgcgc cgggcggtgg 240 agtcagagcc cgggcgcggg agcaggagct gcaagatcag caccagcggc tccggcacct 300 gcaccagctc ccgggccccg cgctgcgctc tccgccccgc cgcactcggg gccgtcgccc 360 cgcgctctct atggatgtca aggcggcccc caacgggtgc cactatcgag gaccggatcc 420 tgcggatcac cggctactat ggctattatc caggttactc cagccagaaa acagacgatg 480 ggacacagac tcattctgag aacagcagcc aagaaaaaca gaatcaaggc tcgctgcctg 540 tcctgcacgt ccatggttct gaagggcatc tggggactct tgatcatctt gtcagtatca 600 tcatcttggt ctattattct ggtcatctag ccactgctca agaaaagcaa tctccaatga 660 aaaaattcag ggaatgcagt cggatttttg gtgaagatgg tctgacgctg aaactctttc 720 ttaaaagaac tgctcccttt tctattctat ggactttgac taattacctt tatttactgg 780 ctttaaagaa gctgacggcc acggatgtct ccgctctgtt ctgttgtaac aaagcctttg 840 tcttcttgct gtcatggatt gtgctgaaag acaggttcat gggagtgagg atagttgctg 900 caataatggc aattaccggc attgtcatga tggcatatgc agataatttc cacgctgatt 960 ccatcatagg agtggcattt gcggtgggct cagcctctac atctgcatta tataaggtct 1020 tgtttaaaat gtttcttgga agtgccaact ttggggaagc tgcacacttt gtctccacct 1080 tgggtttctt caatttgatc ttcatctcct tcaccccagt catcttgtat ttcaccaagg 1140 tggagcactg gtcctctttt gctgctctgc catggggctg tctctgtggg atggcagggc 1200 tgtggctggc cttcaacatc ctggtgaatg ttggggtggt gctgacatac ccaatcctaa 1260 tctccattgg gacagtgctc agcgttcctg gaaatgcagc tgtggatctc ctaaagcagg 1320 aggtgatatt caatgttgtc cgcctggctg ctaccatcat catctgcatt gggtttctgc 1380 tgatgctgtt gcctgaggaa tgggatgaaa tcaccctgag gttcatcaac agcctgaagg 1440 aaaagaagag tgaggagcat gtggatgatg tgactgatcc cagcatacac ctgcggggca 1500 gaggcagagc caatgggaca gtgtctatac cactggctta gagagggaca tattttgaat 1560 gcacgtgtat gtatattctg tgaatataac aaaattttct cactacctgt acactcaaac 1620 gacagtatta actctgaatt tggataaatc atatgtgaaa taatgccaac aataaaagtt 1680 tacatttata tgcttatcaa ggaattggtg taaataatca taatggattt ttttattaaa 1740 acacatttgt ccttgaacaa aaaacacact aacaaaaaca aaaaaaaaac aacatacata 1800 aacacaaaaa caaaaaacaa aca 1823 <210> SEQ ID NO 79 <211> LENGTH: 4308 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1265361CB1 <400> SEQUENCE: 79 tgtattttat ttgtgttcga aagtccgcta attcccaatg tggagggttg gggatgtttc 60 ccttagcgcc tctgggacgc tgtccctaag gccttattcc atgttgaatc tgacgctctc 120 aatgtccagg ctcggctgcg gcgtggggac cgaaaagggg cggggtgggt cggacggcag 180 tttaattacg tccccgggaa ctgcgccgat ttggactttt ggcacttgga cctatgcttt 240 aaaaagaaaa aagtgtcatt ggcgtggagt ggggctagtg gagggtgagg tgaatgcgcc 300 gtttggaaac cacaggacag tgaacgtttc gtctctccca gcgagactct cccgcgggcc 360 cggcggccgc atcgggagcc cggcggaaac atggcggcgc ccggaggccg gggccgcagc 420 ctctccggcc tgctccccgc gcagacctcg ctagagtacg ccctgctcga cgccgttacc 480 cagcaggaga aggacagcct ggtctaccag tatctgcaga aggtggacgg ctgggagcag 540 gacttgtcag tacccgagtt tccggaagga ttagaatggc tgaacacaga agaacctatt 600 tctgtctaca aggatctatg tggaaaaata gtcgtccttg atttcttcac ctactgctgc 660 ataaactgta ttcacctatt gcctgatctc catgcattag aacacacata ctctgataaa 720 gatggtcttc ttattattgg tgttcactcg gctaagtttc caaatgaaaa agtcctggat 780 aacattaaga gtgctgttct tcgatacaac atcacccacc ctatggttaa tgatgcagat 840 gccagccttt ggcaagaact agaagtttcc tgctggccaa ctctagtcat acttggacct 900 cgtggaaaca tgttgttttc tttgattgga gagggacaca aagataaatt atttttatat 960 acttcaattg ctttaaagta ttacaaagac agggggcaga tcagagataa taaaattgga 1020 ataaaactct ataaagattc tttgccacct tcaccattgc tatttcctgg caaagtaaca 1080 gtagaccaag ttactgatag attggtaata gcagacactg gacatcatag aattttggtc 1140 gtttggaaga atggacaaat tcaatatagc attggaggac ccaaccctgg aagaaaagat 1200 ggaatatttt cagaatcaac ttttaattct ccacagggtg tagccataat gaataatatc 1260 atatatgtgg cagacactga aaaccacctt ataagaaaga ttgacctaga agctgagaag 1320 gtgagcactg tagctggtat tggaattcaa ggtacagata aagaaggtgg agcaaaagga 1380 gaacaacaac ccattagttc cccttgggat gtagtttttg gaacatcagg ttcagaggtc 1440 caaagaggtg acattttatg gatagccatg gcagggactc atcagatatg ggcactcctg 1500 ctggactctg gcaaactgcc aaagaaaaat gagttaacaa aaggaacctg ccttaggttt 1560 gctggaagtg gaaatgaaga gaatcgaaac aatgcctatc ctcacaaggc aggttttgcc 1620 caaccttcag gcctttcctt ggcctctgaa gatccctgga gctgcttgtt tgtagcagat 1680 agtgagagca gtacagtgag aaccgtttca ctgaaagatg gagcagtgaa gcacctcgta 1740 ggaggagaaa gagaccccat gaatttattt gcttttggtg atgttgatgg agtaggaatc 1800 aatgcaaagc ttcaacaccc ccttggagta acatgggaca aaaaaaggaa tttactttat 1860 gttgcagact cctacaatca caagattaaa gttgtggatc caaaaacaaa aaactgtaca 1920 acattagcag gaactggaga cacaaataat gttaccagtt ccagttttac agagtcaact 1980 tttaatgaac caggaggctt gtgtattgga gagaatggag aattattata tgtagcagac 2040 accaataatc atcaaattaa agtgatggat ttagaaacta aaatggtatc tgtgctcccc 2100 atcttcagat ctgaaaatgc tgtggtagat ggcccgttcc tagtagaaaa acagaagaca 2160 ttacccaaac tacctaaatc tgctccaagc attaggcttt cccccgtgac tgcgtgtgct 2220 ggccagactc ttcagttcaa actcagatta gacctcccat caggatcaaa gctaactgaa 2280 ggagtatcca gttgctggtt tctaacagct gaaggcaatg aatggctact tcaaggacag 2340 atagcagctg gagatataga gaacatttcc agtcaaccaa caatttcact acaaattcct 2400 gatgattgct tatcacttga agccattgta tctgtcagtg tgtttcttta ttactgtagt 2460 gcagacagca gtgcttgtat gatgaaggca attttgttca gtcagccttt acaaataacg 2520 gatacacagc aaggttgcat agctccagta gagctcaggt atgtatttta gccagccagc 2580 tagctagcaa cccattgcca ccacctactg tctcccatcc tgactatcac tgtaatttaa 2640 ggaaagaaaa cttcagttct gcctctggat accaagatgc ccattgctca gttcagacaa 2700 ctgatattaa aataaagcta tgctccttac ttacttcttt tattataaac aaattccttt 2760 gctttggctg atactagctg agtcattgat catcattggt accatgatat tgtaatctat 2820 gctgctattt ggcacaagac tgaagttcac actacagtag agaatactat aagataattt 2880 gcaataaata ctgataataa taataccaga tattttaact aactttttct acctttatta 2940 atagcaatca gcacacttga atgtgtaaat ttcacagtaa ctttaggcag aacttaagct 3000 ccaggccaca tttgtataag aacaccaagt attcaaggca taaagtctgt tgtaagccaa 3060 aaaaaagtct tttcatcact gtagaagctt aaggagtaca tcagtggtaa atacgatctt 3120 tattctcttc tgtggttttc tcagttgaga tatttttaaa agagagtttt gatctatttt 3180 tattataaat tatttgttat ttaacatacc attatgaatg ccttaaaact ttgtacagat 3240 aaagttggac atagaatctc taaggactga ctcctttaac tgtttttgag tgactacatt 3300 accagataat gaatgagtcc ccagaaatat tatgactttc aaggaaaaag ggactttagg 3360 acacattact tagtgtctgt gataaataat ttattgtgac agctaaatct gatggttaca 3420 tatcttgttt tggaaatgta catttcactt gtaagcatta aatgcagatt tgttgagttt 3480 aggttttgag gtttttttcg ttcccatatt cagaatttaa attatgatca tttattgtga 3540 tgtttttaaa aatcactttt aagccttaaa agtgaaattt tcagtgtgag gtgctttcat 3600 gctattaata gatacagtat atcctaatat attagtcttc aaaatattaa ggccgaaaca 3660 gtgatttaat gatactattt tttaattttt gttgtttttt atccctaaaa aaagatattg 3720 gaaaggtttt ttttctattg gtcataattt ataactactt aaaagcctaa tcttgttttc 3780 cttaagacct attcaacatg tttgtgattt aatcagctta caagggttta aaaacatcag 3840 gtgaaccatg tttatttatt cagtaaatat ttatagacaa tatggcataa tatgcttccc 3900 ttccctgtaa aaacagtgct aaatttgaag tgtaatcttt tttaaacatc attgtctatt 3960 tttaattttg tttgaaatgt agtattagtt tgttttattc ataaggttag ctgaatctct 4020 gaagtaagga tgtataaatc atgacattga tttaattagt catctactga agctactttt 4080 aaagagaaat atagatataa aattaaaagg aatcctgttt aaaattatat gtaattacct 4140 cataaacctt ttctctccac aagcaatcaa aaaaatgaaa tgttctgtaa taaaagggtg 4200 tataacatac tctcttttat gagaataggc cttagttatt ttattttatt tttgagacag 4260 gagaatatca cttgaacgtg ggaggtggag actgcaccac tgcattat 4308 <210> SEQ ID NO 80 <211> LENGTH: 5142 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2645814CB1 <400> SEQUENCE: 80 gcatgacaag gtgctggcgc aagatttccg ccctccatga atagctgatc ccgcggacca 60 ctgggttgcc aagctcgcgc cggatgcgga gcgcggtgct gccggtggag cttcaggtct 120 tgatagactt tctgtaaaga aggaatgatt tggtgatgga gtgttcccac tgaccgatgg 180 actcaaagaa gagaagctca acagaggcag aaggatccaa ggaaagaggc ctggtccata 240 tctggcaggc aggatccttt cccataacac cagagagatt gccaggctgg ggaggaaaga 300 ctgttttgca ggcagccctc ggagtgaaac atggagttct tctgactgaa gatggtgagg 360 tctacagctt tgggactctt ccctggagaa gtggaccagt ggagatttgt ccaagtagcc 420 ccattctaga aaatgccctg gttgggcaat atgttattac tgtggcaaca ggaagcttcc 480 atagtggagc agtgacagac aatggtgtcg cgtacatgtg gggagagaat tctgctggcc 540 agtgtgcagt agccaaccag cagtatgtgc cggaaccaaa tcctgtcagc attgctgatt 600 ctgaggccag ccctttgtta gcagtcagga ttttacagtt ggcgtgtggc gaggagcaca 660 ctctggcatt gtcaataagc agagagattt gggcatgggg taccggttgt cagttgggtc 720 tcattaccac tgccttccca gtgacaaagc cgcaaaaggt agaacatctt gctgggcgag 780 tggtgcttca agttgcctgt ggtgctttcc acagcttagc ccttgtacaa tgcctccctt 840 cccaggatct gaagccagtc ccagaacgat gcaaccagtg cagccagctc ttgattacta 900 tgactgacaa agaagaccat gtgattatat cagacagtca ttgttgccca ttaggtgtga 960 cactgacaga atctcaggca gaaaaccatg ccagcactgc tctcagcccc tccactgaaa 1020 cccttgacag gcaggaagaa gtatttgaga acactcttgt agcaaatgat cagtctgttg 1080 ctactgaact gaatgcagta agtgctcaga tcacaagcag cgatgccatg tcctctcaac 1140 aaaatgtcat gggaacaact gaaatttcct ctgccagaaa cataccatca taccctgaca 1200 cccaagcagt caatgaatac ctacggaaac tgtcagatca ttcagtaaga gaggactcag 1260 agcatggtga aaagccagtg ccatctcagc ctcttttaga agaagcaatt cctaatctcc 1320 acagcccgcc taccacaagc acctcagccc taaacagcct ggtggtctct tgtgcatctg 1380 ctgttggtgt gagagtggct gctacttatg aagctggtgc cttgtcactg aagaaagtta 1440 tgaactttta tagtacaacc ccttgtgaaa ctggagctca ggcaggcagt agtgccattg 1500 gccccgaagg tttgaaagat agcagggaag aacaggttaa acaggaatca atgcaaggaa 1560 agaaaagttc aagtcttgtg gatatcagag aagaagaaac agagggaggc agtcgaagac 1620 tctccctccc tggattgttg tcacaagttt cccccaggct cttaagaaag gctgcacggg 1680 tgaaaacgag gacagtggtt ctgaccccca catacagtgg agaagcagat gcgctcctgc 1740 cttctctgag aacagaagtg tggacctggg ggaaagggaa ggaagggcag ctggggcacg 1800 gcgatgttct gcctaggctt caaccgttgt gtgtaaaatg tctggatggc aaagaagtaa 1860 tccatctgga ggcaggtggt taccattctc ttgcacttac tgcgaaatcc caggtttact 1920 catggggtag caataccttt ggtcaacttg ggcattccga ttttccaaca acagttcctc 1980 gtcttgcaaa gataagcagt gaaaatggag tctggagcat agctgcaggc agggattatt 2040 ccctgttttt agtggataca gaagacttcc agcctgggtt atattacagt ggccgacagg 2100 accctacaga aggtgacaac cttccagaga atcacagtgg ttctaagact ccagtacttc 2160 tctcctgtag taagcttgga tatataagca gagtgacagc aggaaaagat agctatttag 2220 ccttggtgga taaaaacatt atggggtata ttgccagtct ccacgagtta gctactacag 2280 aaagacgatt ctattcaaaa ctaagtgata tcaaatctca gattctcagg cctcttctca 2340 gtttagaaaa tttgggcact acaactacag tccagctgtt gcaggaggtg gctagccgat 2400 tcagcaagct gtgttacctc attggtcagc atggagcctc attgagcagc ttccttcatg 2460 gggtaaagga agccaggagt ttggtcatcc tgaagcattc aagtctcttc ttggatagtt 2520 atacagagta ttgcacatct attacaaatt tcctggttat gggaggattc cagcttcttg 2580 ctaagcctgc cattgatttc ctaaataaaa accaagagct gttgcaagat ttgtcagaag 2640 tgaatgacga aaacactcag ttgatggaaa tactgaatac tttgtttttc ttgccaatca 2700 gacgacttca taattacgca aaagttttgc taaagcttgc tacttgtttt gaagtggcat 2760 ctccagaata tcagaaactg caggattcca gttcttgtta tgagtgtctt gctctccatc 2820 tcggcaggaa aaggaaggaa gcagaataca cactgggctt ctggaagacc ttccccggaa 2880 aaatgacgga ttccttgagg aagccagagc gtcgactgct gtgtgagagt agtaaccgag 2940 ccctgtctct gcagcatgct gggaggtttt ccgtgaattg gttcattctc tttaatgatg 3000 ccctggtcca tgcccagttc tccacgcacc atgttttccc tctggccacg ctgtgggcag 3060 agccactgtc tgaagaagct ggtggtgtga atggcttaaa gataactaca cctgaggagc 3120 agttcactct catttcatct acaccccagg aaaagacaaa gtggctacga gctataagcc 3180 aagccgtaga tcaggctttg agagggatgt ctgatctccc cccttatgga agtggtagca 3240 gtgttcagag acaggaacca cccatttcac gcagtgccaa atatactttc tacaaggatc 3300 ctcgcctaaa ggatgccacc tatgatggac gctggctttc agggaagcct catggcagag 3360 gggttttgaa gtggcctgat ggaaagatgt attctggcat gttcaggaat ggcttggaag 3420 atgggtatgg agaatacaga atcccaaaca aggcaatgaa caaagaagac cattatgtgg 3480 gccattggaa agaaggaaaa atgtgcggtc aaggagtcta cagctatgct tctggtgaag 3540 tatttgaggg ctgttttcaa gataatatgc gtcatggtca tggtcttcta cgaagtggga 3600 aattgacgtc ctcttctcct agtatgttca ttggccagtg ggtaatggat aagaaagcag 3660 gatatggtgt ctttgatgat atcactaggg gggaaaagta tatgggaatg tggcaagatg 3720 atgtgtgtca agggaatggt gtggtggtta cccagtttgg attatactac gagggcaact 3780 ttcaccttaa taaaatgatg ggaaatgggg ttttgctttc cgaagatgat actatctatg 3840 aaggagaatt ttcagatgac tggactctta gtggaaaggg aacactgact atgccaaatg 3900 gagactacat tgaaggttat tttagtggag aatggggatc tgggataaaa atcactggaa 3960 cctacttcaa acctagtcta tatgagagtg ataaagacag acctaaagtt ttcaggaagc 4020 taggaaacct ggcagtgcca gctgatgaga agtggaaagc ggtgtttgac gaatgttggc 4080 gccaactggg ctgtgagggc ccaggccaag gggaagtttg gaaagcatgg gacaatattg 4140 ctgtggcctt gaccaccagt cggcgccagc acagagacag tccagaaata ctgagtcgtt 4200 cacagactca gacactagag agtttggaat tcattccaca gcatgttggt gccttctctg 4260 tggagaaata tgatgacatc aggaaatatt taataaaggc ctgtgacact cctctgcacc 4320 ccctgggcag gcttgtggag acactggttg cagtgtatag aatgacatac gtgggcgtag 4380 gagccaaccg caggttattg caggaggctg taaaggagat taagtcctat cttaagcgaa 4440 ttttccagct ggtgaggttc ttatttcctg agctgcctga agaaggcagc acaattcctc 4500 tctctgctcc tctgccaacc gaaaggaagt ctttttgcac tgggaagtca gattcccgat 4560 ctgaatcacc agagccaggt tatgtagtaa cgagttctgg attattgctt cctgtgctgc 4620 tacctcggct ctacccaccg ctgtttatgc tttatgcttt ggataatgat cgcgaggaag 4680 acatttactg ggaatgtgtc cttcgactaa ataagcagcc agatattgct ctcctgggct 4740 ttcttggggt gcagaggaaa ttttggccag caaccttgtc aatccttgga gagagtaaaa 4800 aggttttgcc aaccacgaaa gatgcttgtt ttgcctcagc agtagaatgt ctgcagcaga 4860 tcagcacaac atttacccca tcagacaaac ttaaggtcat ccagcagact tttgaggaga 4920 tctctcagag tgtcctggcg tcactccacg aagacttctt gtggtccatg gatgacttgt 4980 ttcctgtttt cttatatgtg gtgctacggg ccaggattag gaatttaggc tctgaggtac 5040 acctcattga ggatctaatg gacccctatc ttcagcatgg ggaacagggt ataatgttca 5100 ccaccttgaa ggtgagtata gttattattt aatactttct ta 5142 <210> SEQ ID NO 81 <211> LENGTH: 4287 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 695481CB1 <400> SEQUENCE: 81 tcatggagtt tgccacaaga tgttgttgac ggaacgtgtg tagcagtaaa taacaagtat 60 cgactaatgg catttggctg tgtgagtggt tctgtgcagg tctatacaat agataacagc 120 actggagcca tgctgctacc tcataaatta gagctaacag caaacagtat cctgacattt 180 ggaataaaac aggagctgtt aaattgatga gatggtctcc tgacaatagt gttgtaatag 240 tgacctggga atacggaggc ctttctttat ggagtgtttt tggagcacag ctgatttgta 300 cacttggagg agattttgct tataggtctg atggcaccaa aaaagatccc cttaagatca 360 actctatgag ctggggtgca gaaggctatc acctatgggt aatcagcgga tttggttctc 420 aaaacactga aattgagtct gacctcagga gtgtagttaa acagcccagc atcctgttat 480 ttcagtttat taagagtgta ctcactgtaa acccttgtat gagtaaccaa gagcaggtgt 540 tgcttcaggg tgaggatcgc ttgtacttga actgtggaga ggcttcacaa acccagaatc 600 ccaggagttc ttcaacacac tctgagcata agcccagtcg agaaaagagc ccatttgcag 660 atggaggttt agagtctcag ggattaagca ctttacttgg acatcggcat tggcatgttg 720 tacagatttc cagcacctat ctagagagca attggcctat acggttttca gctattgata 780 agcttggaca gaatattgct gtggttggca agtttggttt tgcacattac tctttactca 840 ccaaaaaatg gaaacttttt ggaaacatta cccaggagca aaatatgatc gtgacaggtg 900 gcttagcctg gtggaatgat tttatggtcc ttgcgtgtta taacataaat gaccgtcaag 960 aagagcttag agtatacttg cgaacatcaa atctggacaa tgcctttgct catgtcacca 1020 aagcacaagc agaaacatta ctgcttagtg tcttccagga catggtaata gtatttagag 1080 cagactgttc aatatgcctt tacagtattg aaagaaaatc tgatggtcca aatactactg 1140 ctggtattca agttcttcag gaggtttcca tgtcacgcta cattcctcac cctttcctgg 1200 tggtatctgt cactctgaca tcagtgagta cagagaatgg aatcaccttg aaaatgccac 1260 agcaggctcg tggtgcagag agcattatgt taaacctggc aggacagctc atcatgatgc 1320 agagggacag gtcaggccca cagatccggg agaaggacag taaccctaat aaccaaagga 1380 aacttctgcc attctgtcct cctgttgtac tagcccagtc tgttgaaaat gtctggacaa 1440 cgtgtcgagc aaataaacag aaacgtcacc ttctggaggc cctctggctg agctgtggtg 1500 gtgcagggat gaaagtttgg ctccctctct tccctaggga tcaccgcaag ccccattcct 1560 tcttgtccca gcggatcatg ctgcctttcc acatcaacat ttacccgcta gctgttctgt 1620 ttgaagatgc tttagtcctt ggtgctgtca atgacacttt gctctatgat tctttatata 1680 ctcggaacaa tgctagagaa cagctggagg tgctcttccc tttctgtgtt gtggagagaa 1740 cctctcagat ctacctccac cacattctac gtcaacttct ggtcagaaac cttggggagc 1800 aagccttgct cttggcccag tcctgtgcca cattacctta cttccctcat gtgctggagc 1860 tcatgctcca tgaagtactg gaagaagaag ctacctcacg ggagcccatt cccgaccctc 1920 tgcttcccac tgtggcaaaa tttatcactg agttccccct cttcctgcag acagttgtcc 1980 attgtgccag gaagaccgaa tatgccctgt ggaattacct ttttgcagct gttggaaacc 2040 ctaaggactt gtttgaggag tgtttgatgg ctcaggattt ggacacagct gcctcttacc 2100 ttattatctt acagaatatg gaagtccctg cagtaagtag gcaacatgct acccttctat 2160 tcaacacagc actagaacaa ggcaagtggg acctttgtcg acacatgatt cgatttctta 2220 aagccattgg ctctggagaa tctgagacac ctccatccac acccacagct caggaaccca 2280 gttcaagtgg tggatttgag ttcttcagga atcgaagcat cagtttatcc cagtcagctg 2340 aaaatgttcc tgccagtaaa ttcagtttac agaaaacact aagtatgcca tctggtccct 2400 ctggaaaaag atggagcaaa gacagtgact gtgctgagaa catgtatatt gacatgatgc 2460 tctggagaca tgctcggcgc ctcttagaag atgtgaggtt aaaggacctt ggctgctttg 2520 cagcccagct gggctttgaa ctaattagtt ggctatgcaa ggaacgtacc cgagccgccc 2580 gggtagacaa ctttgtaata gccctgaaga gactccacaa agatttcctg tggccacttc 2640 caatcatccc agcctcttct atcagttctc ctttcaaaaa tggaaaatac cgaactgtgg 2700 gagagcagct gttaaagtct caatcagctg acccattttt gaaccttgag atggatgctg 2760 gcatctccaa catccagcga agtcagagct ggctcagcaa cattggcccc acccatcatg 2820 agatagacac agcttcatcc catggaccac aaatgcaaga tgccttcttg tcacctttat 2880 ctaataaagg tgatgaatgc agtattggtt cagccacaga cttgactgaa agtagctcca 2940 tggtggatgg cgactggaca atggtggatg aaaatttctc tacactcagt ttaactcagt 3000 cagagctgga gcacatttcc atggagttgg ccagtaaagg gcctcataaa tcccaggtcc 3060 agcttcggta tttgctacac attttcatgg aggcagggtg cctagactgg tgcatcgtta 3120 taggcctgat tcttagagaa tcctcaataa tcaatcagat tttggttatt acacagtctt 3180 cagaggtaga tggagagatg ttacagaaca taaagacagg gctccatgca gtggaccgat 3240 gggcctctac agactgtcct ggatataagc catttttaaa catcattaag ccacaactgc 3300 agaagctcag tgagataaca gaagagcagg tccagccaga tgccttccaa ccaataacta 3360 tgggtaagac tccagaacag actagccccc gggcagagga gagcaggggc tcctccagcc 3420 atggaagcat cccccagggt gaagttggaa gcagcaatat ggtcagccgg aaagaggagg 3480 acacagccca agcagaggag gaagaacctt ttcaggatgg gacgtacgac tgttctgtgt 3540 cctaacagtg aggttccatc acaaaggggc agtattaatt agcagcagcg tgcagctcag 3600 tacgttgtaa catagttgga tgatttaaca ggagaactca gttcagagac tcttcggtaa 3660 gtattagtag attttaacta attctttctt gtctaagaaa tctttttgac tccataaaaa 3720 tgtgatataa agcatctttc ataaaaaaat tttaagctgc agtgaaaagt aaatattgta 3780 cagatgtaca tgagaatatt tggttttact caaaggttgg tagctcttaa accacaggaa 3840 ttgttttgcc ccaggtgagc ttactttttc actacttaca tcttctcaca tttcccggtt 3900 ctgcattatg tccagattgc tttttaaaaa ataaatgcta aggtgcttgc tatagtctgt 3960 caggtacttg agctacctgt ttgctccctt ggatacagct ggactcttta atcagtcctc 4020 ctgaatagat tgctaccctg gggcacaata tgtgccagtg tgatggaaac attctccttg 4080 gctttactag ccagtcaaat cccagtccag aattgatgga agctatttac ctgtgagtta 4140 atgtgcttgt tttagcaagc ttgattccca ttagaccaat gtgggcagag gtctgagggg 4200 ggttcttctt caattttgct gttaggatac ccactaaact attttgtatt taaagaacag 4260 tatccttttt gtggaatatt cttgttt 4287 <210> SEQ ID NO 82 <211> LENGTH: 3437 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 699941CB1 <400> SEQUENCE: 82 ctaaaacgct aataatttat tagatctaaa gccccgcccc gccccaaccc ggggctccga 60 gccggagccg agtctgcgcc tgggggtgag tacgcgaccc ctacccagcc ctcgctcttt 120 tcttcgaaga tcccaccacc acccaaagaa aaaacctgga ctcagctgcg cgtcccctcc 180 cttcaacctc ctgcgggacc cagaggtgcc cgggcccgcg ggacccaggg gtggcgcgcg 240 ctgcccccaa ccccgcacca tcccgagcca aatgaggacc atgcggcagt agcagccatg 300 ctgccctttc tgctggccac actgggcacc acagccctca acaacagcaa ccccaaggac 360 tactgctaca gcgcccgcat ccgcagcact gtcctgcagg gcctgccctt tgggggcgtc 420 cccaccgtgc tggctctcga cttcatgtgc ttccttgcac tgctgttctt attctctatc 480 ctccggaagg tggcctggga ctatgggcgg ctggccttgg tgacagatgc agacaggctt 540 cggcggcagg agagggaccg agtggaacag gaatatgtgg cttcagctat gcacggggac 600 agccatgacc ggtatgagcg tctcacctct gtctccagct ccgttgactt tgaccaaagg 660 gacaatggtt tctgttcctg gctgacagcc atcttcagga taaaggatga tgagatccgg 720 gacaaatgtg ggggcgatgc cgtgcactac ctgtcctttc agcggcacat catcgggctg 780 ctggtggttg tgggcgtcct ctccgtaggc atcgtgctgc ctgtcaactt ctcaggggac 840 ctgctggaga acaatgccta cagctttggg agaaccacca ttgccaactt gaaatcaggg 900 aacaacctgc tatggctgca cacctccttc gccttcctgt atctgctgct caccgtctac 960 agcatgcgta gacacacctc caagatgcgc tacaaggagg atgatctggt gaagcggacc 1020 ctcttcatca atggaatctc caaatatgca gagtcagaaa agatcaagaa gcattttgag 1080 gaagcctacc ccaactgcac agttctcgaa gcccgcccgt gttacaacgt ggctcgccta 1140 atgttcctcg atgcagagag gaagaaggcc gagcggggaa agctgtactt cacaaacctc 1200 cagagcaagg agaacgtgcc taccatgatc aaccccaagc cctgtggcca cctctgctgc 1260 tgtgtggtgc gaggctgtga gcaggtggag gccattgagt actacacaaa gctggagcag 1320 aagctgaagg aagactacaa gcgggagaag gagaaggtga atgagaagcc tcttggcatg 1380 gcctttgtca ccttccacaa tgagactatc accgccatca tcctgaagga cttcaacgtg 1440 tgtaaatgcc agggctgcac ctgccgtggg gagccacgcc cctcatcctg cagcgagtcc 1500 ctgcacatct ccaactggac cgtgtcctat gcccctgacc ctcagaacat ctactgggag 1560 cacctctcca tccgaggctt catctggtgg ctgcgctgcc tggtcatcaa tgtcgtcctc 1620 ttcatcctcc tcttcttcct caccactcca gccatcatca tcaccaccat ggacaagttc 1680 aacgtcacca agcctgtgga gtacctcaac aaccccatca tcacccagtt cttccccacc 1740 ctgctgctgt ggtgcttctc ggccctcctt cccaccatcg tctactactc agccttcttt 1800 gaagcccact ggacacgctc tggggagaac aggacaacca tgcacaagtg ctacactttc 1860 ctcatcttca tggtgctgct cctaccctcg ctgggactga gcagcctgga cctcttcttc 1920 cgctggctct ttgataagaa attcttggct gaggcagcta ttcggtttga gtgtgtgttc 1980 ctgcccgaca acggcgcctt cttcgtgaac tacgtcattg cctcagcctt tatcggcaac 2040 gccatggacc tgctgcgcat cccaggcctg ctcatgtaca tgatccggct ctgcctggcg 2100 cgctcggccg ccgagaggcg caacgtgaag cggcatcagg cctacgagtt ccagtttggc 2160 gcagcctacg cctggatgat gtgcgtcttc acggtggtca tgacctacag tatcacctgc 2220 cccatcatcg tgcccttcgg gctcatgtac atgctgctga agcacctggt agacaggtac 2280 aatctctact acgcctacct gccggccaag ctggacaaga agatccactc gggggctgtg 2340 aaccaggtgg tggccgcgcc catcctctgc ctcttctggc tgctcttctt ttccaccatg 2400 cgcacggggt tcctagctcc cacgtctatg ttcacatttg tggtcctggt catcaccatc 2460 gtcatctgtc tctgccacgt ctgctttgga cacttcaaat acctcagtgc ccacaactac 2520 aagattgagc acacggagac agatactgtg gaccccagaa gcaatggacg gccccccact 2580 gctgctgctg tccccaaatc tgcgaaatac atcgctcagg tgctgcagga ctcagaggtg 2640 gacggggatg gggatggggc tcctgggagc tcaggggatg agcccccatc atcctcatcc 2700 caagatgagg agttgctgat gccacccgac gccctcacgg acacagactt ccagtcttgc 2760 gaggacagcc tcatagagaa tgagattcac cagtaagggg agggaggggc cctggaggcc 2820 acatcctgcc ccaccccacc cccactccca cggacactaa aacgctaata atttattaga 2880 tctaaagccc cttcctcccc agcccctgct ttcattaagg tatttaaact tgggggtttc 2940 actgctctcc cccatgatgg agggagggag ccccccaacc tcagtgagga gagccccgag 3000 ccggccccgg ggcaaagagg ggtgcagagg gagttccccc agatcagtac cccccacccc 3060 tccccagcta gtagcatgac caggagaggg ttaatgagag ccaagaggag tacctggtgc 3120 acctggtgcc ggtggctgga gacctggggg gcaggtggat ctggggctgt tcccccccct 3180 ccgttttttc caccccacag ttcctcctgg gatctggccc tccagggaag tggagcctcc 3240 agcccctagg ggatgcatga ggggggaggg ggtgctgagt gggaggaaga gtcaggctca 3300 cagctggggt ggcctggggg tgggggtggg caaggctgac actggaaaat gggtttttgc 3360 actgtttttt ttttggtttt tttgttcttt tttgtttttt tcctttaaaa taaaaacaaa 3420 gaaaagctca aaaaaaa 3437 <210> SEQ ID NO 83 <211> LENGTH: 3063 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 1515839CB1 <400> SEQUENCE: 83 cccacgcgtc cgcccacgcg tccggcggag ctcctgggct gcagctcctg gagtttccga 60 ggttcgtgcg cgtctggtgg cggcggcgtg atgttctcgg caggagcgga gagtttgctc 120 caccaggcca gggagatcca ggacgaggag ctgaagaagt tctgttcccg gatctgtaaa 180 ctgctgcagg cggaggactt ggggccggac accctcgact ccctgcagag gctcttcctc 240 atcatctcag ccacgaagta cagccggagg ctggagaaga catgcgtaga cctgctgcag 300 gccaccctcg gcctgcctgc atgccccgag cagctccagg tgctttgcgc cgccatcctg 360 cgagagatgt ccccctctga cagcctcagc ctggcctggg accacacgca gaacagccgg 420 cagctgagcc tggtggcctc cgttctcttg gcccagggtg acagaaacga ggaggtcaga 480 gccgtgggcc agggcgtgct acgagcgctg gagagccggc agcctgaggg acccagcctc 540 agacacctcc tccccgtcat ggccaaggtc gtggtcctca gcccgggcac cctccaggag 600 gaccaggcca ccctgctcag caagcggctg gtcgactggc tgcgctacgc cagcctccag 660 caagggctcc cacactccgg cggcttcttc tccacgccca gggcccggca gccgggcccc 720 gtcaccgagg tggacggggc ggtagccaca gacttcttca cggtgctctc cagcggccac 780 cgcttcacag acgaccagtg gctgaacgtg caggccttct ctatgctgcg ggcgtggctg 840 ctgcacagcg gccccgaggg cccgggcacc ctggacacag atgacaggtc agagcaggag 900 ggctccactc tgtcggtgat ctccgccacc tcctctgccg gccgcctgct gccgccccgg 960 gagcggcttc gggaggtggc cttcgagtac tgccagcgcc tcattgagca aagtaaccga 1020 cgagccctga ggaaggggga ctccgacctg cagaaagctt gcctggtgga ggccgtgctg 1080 gtgctggacg tgctgtgccg gcaggacccg tccttcctgt accgaagtct ctcctgcctg 1140 aaggccctgc acgggcgggt gcgcggggac ccggcctctg tgcgggtgct gctgcccctc 1200 gcccacttct tcctgagcca cggggaagcg gctgcagtgg actcggaagc cgtctaccag 1260 cacctgttca ccaggatccc ggtggagcag ttccacagcc ccatgctggc ctttgaattc 1320 atccagttct gcagggacaa cctccacctg ttcagcgggc acctcagcac cctcagattg 1380 agcttcccca acctctttaa gttcctggcc tggaacagcc cacccctcac ctccgagttt 1440 gtggcgctcc tcccggccct ggtggacgct ggcacagccc tggagatgct gcacgcgctg 1500 ctggacctgc cctgcttgac ggcggtgctg gacctgcagc tcaggtcagc accggctgca 1560 tccgagaggc cactctggga cacctctctc agggccccca gctgcctgga ggccttccgg 1620 gacccgcagt tccagggtct tttccaatac ctgctgcgcc ccaaggccag tggcgccact 1680 gagaggttgg cgccactcca ccagctgctg cagcccatgg ccggctgtgc ccgcgtggcc 1740 cagtgtgccc aggccgtgcc cacgctgctg caggcattct tctcagcagt gacccaggtg 1800 gctgacgggt ccctgatcaa ccagctggcg ctgctgctcc tgggcaggag cgactcgctc 1860 tacccggccc cagggtacgc tgccggtgtg cacagtgtgc tgagttctca gttcctggcc 1920 ctgtgtacgc tgaaaccctc cctggtggtg gagctggcaa gagacctgct ggagttcctg 1980 ggcagcgtga atggtctctg cagcagggcg agcctcgtca ccagcgtggt gtgggccatc 2040 ggcgagtacc tgtcggtgac ctacgatcgg aggtgcaccg tggagcagat caacaagttc 2100 ttcgaagccc tggaggctct gctattcgag gtcacccagt gccgcccctc tgctgccctg 2160 cccaggtgtc ccccccaggt ggtcaccgtg ctgatgacca cgctgacgaa gctggcctcc 2220 cggagccaag atctgatccc cagggcctct ttattgctgt caaagatgag gaccctggct 2280 cacagtccag ccaccagctc cacgcacagc gaggagggcg cggaagccat ccgtacccgg 2340 gccacagagc tgctgaccct gctgaagatg cctagcgtgg cccagtttgt gctcacaccc 2400 agcacggagg tgtgcagccc ccgctatcac cgcgatgcca acacggccct gcccctggcc 2460 ctgcgcacgg tcagccggct ggtggagagg gaggccggcc tcatgccagg gtgaagggac 2520 agtggccagg gacttcggtg cagattaaga gcctgggcag ccagcttgct actgaggcca 2580 ggctgatagg agctcaggag ggcgcgggag tcctgggaga ggaggcaagg cccacggtgg 2640 gcttggcacc ctcacagaca cgcggggctg gcccccctgc tcaccctctg ggctttgtct 2700 ccgagccttt tgctcccagg caacactgag ctgagctgag gggtgccatg gagcggctct 2760 gattggaggc ttgaggccct gtggctgggt cgggtggagg ctgctgggtc tgtttcctag 2820 tcttttgttt ttggacagtt gatgggcaag aagagctgca gtaaaagtaa atctccttta 2880 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaacaaaa 2940 aaaaaaaaaa aaaaaaaaaa acaaaaaaaa aaaaaaaaaa aaaaaaagac gggagggggg 3000 ggggacaaga cgagagccgc caccggtggc gcgcgcgccg ccgccccgaa acacacaaga 3060 agc 3063 <210> SEQ ID NO 84 <211> LENGTH: 2512 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 2300766CB1 <400> SEQUENCE: 84 gcgccccgcc ccccaggagg ccgcaccctg cgccagggcc cggagacagc aacatcttct 60 ggggcctgca ggagacctga cagatgccaa aacaaaggaa cagttgggat ccaggcagca 120 tgaggtagaa tggcaaacct accagggtat tctgaagaag acaagagtca tggaaaaaac 180 caagtggctg gatatcaaag gaaatcatgg aaatattctg ctgtacgtag agatggctct 240 ttccattatg tccacagtac tccctttggc aactattcgt tcatctgtgt agatgccact 300 gtaaatccag ggcctaagag accctataat ttctttggaa ttttagataa gaaaaagatg 360 gaggagctct tattactggc caaggaaagc agtcggagca accatacaat ttggtttgga 420 cactttacaa catccactat tctttctcca tcaccaggaa tccggtcaat aatgagttcg 480 gctatagctt atttgtgtgg acatctccat acacttggtg gactgatgcc tgttttgcac 540 actcgtcact tccagggcac tttggaactt gaggtgggag actggaagga taataggagg 600 taccggattt ttgcttttga tcacgacctc tttagctttg cagatttgat ctttgggaag 660 tggcctgtgg ttcttatcac caatcctaaa tcactccttt atagttgtgg tgaacatgaa 720 ccactagaaa gacttcttca ctcaacacac atcagagtct tggccttttc cttatcctcc 780 attacttctg tcacagttaa gattgatgga gttcatttag gccaggctgt tcatgtgtct 840 ggtcccattt tcgtactgaa gtggaatcct agaaactaca gtagtgggac acataacata 900 gaagtaatcg tccaggattc tgctggaaga agtaagagtg ttcaccacat attttctgtt 960 caagagaata atcatctcag ttttgatccc ctggcatcat ttattctccg tactgatcac 1020 tacatcatgg cccgggtcct ttttgtgctg attgtgctga gccagctcac cattctcatt 1080 atttttagat atcgaggata cccagagctt aaagaacctt cagggtttat aaatctgacc 1140 tcattttctc ttcatgtctt gagcaaaata aacatcttct actattctgt gttgttgttg 1200 accctgtata cagtgctggg tccatggttt tttggtgaaa tcattgatgg caaatttggt 1260 tgctgctttt cctttgggat atttgttaat ggacatttcc tacaaggcag cataacattt 1320 ataattggaa ttctccagct ggcgtttttt aacatcccct tgatggctta catgtgttgg 1380 agcttgctgc agcggtgctt tggtcacaac ttcaggtctc atctccatca aagaaaatac 1440 ttgaaaatta tgcctgttca cctacttatg ctactgctgt acatctggca ggtttattcc 1500 tgctactttc tttatgcaac atacggcacc ctagcttttt tattctcccc tttgcggacc 1560 tggttgacac tgctgacacc tgttctcatt cgttatgtgt ggacactgaa ctccaccaag 1620 tttggaatct tcatggtgca gttaaaaagc cacctgagct cctgaaggcc atgtctcacc 1680 actggcagct gggcagaagc ccagcctctg tgtctgtagc ccaggcctct accccagtag 1740 caggtggagg gccaggattg gtgggtgagc tttagggagc agctgctcgt ttggagtcct 1800 ggacgttgga gggattaccc actactgata cctgcagaat ggactgcaga aaagtctcaa 1860 aaataatgcc tttattcctt ccctccctaa ggaggcaaag agttgattta cctttgtgaa 1920 gagaaaaccc ttatctagga catccacagg gtagaggtgg gtgtgtgtac gggagtgtct 1980 gaggcccagt gtgtttttta gggttacccc atgtaaagca cttaccgctg tgcttggaat 2040 tcagcagctg tcaaaggtgc aatttcaggg gcagggaacc tttgaggatc tgggcccgac 2100 cctcactacc cctgagatat tagttcccag gcctgttttc ccacaggatt gtgggctctc 2160 tgcttcctta gtcggaagtg ttttcaacta atcaaataaa tgaaatgaat gatgaataag 2220 aaaaaacaca gacccaaagg gggggccgcc gaactatggg agcctcggtc gacccggggc 2280 aataagttcc ggaccggacc cgtgacggga gttttcccag acaacagggg gaagaatatc 2340 gaatcgggcg gtcttcccat atagtgcgct cgtatcactt gcgataggcc aggtaacctg 2400 attagaaacc tgggaacagg cgacacaagc cgaaacagaa cacacacaca acaggaagtg 2460 acctaacacc gtctgatagc gagtgcccac aacacacggc aacgacacac ag 2512 <210> SEQ ID NO 85 <211> LENGTH: 2407 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7505816CB1 <400> SEQUENCE: 85 gcgccccgcc ccccaggagg ccgcaccctg cgccagggcc cggagacagc aacatcttct 60 ggggcctgca ggagacctga cagatgccaa aacaaaggaa cagttgggat ccaggcagca 120 tgaggtagaa tggcaaacct accagggtat tctgaagaag acaagagtca tggaaaaaac 180 caagtggctg gatatcaaag gaaatcatgg aaatattctg ctgtacgtag agatggctct 240 ttccattatg tccacagtac tccctttggc aactattcgt tcatctgtgt agatgccact 300 gtaaatccag ggcctaagag accctataat ttctttggaa ttttagataa gaaaaagatg 360 gaggagctct tattactggc caaggaaagc agtcggagca accatacaat ttggtttgga 420 cactttacaa catccactat tctttctcca tcaccaggaa tccggtcaat aatgagttcg 480 gctatagctt atttgtgtgg acatctccat acacttggtg gactgatgcc tgttttgcac 540 actcgtcact tccagggcac tttggaactt gaggtgggag actggaagga taataggagg 600 taccggattt ttgcttttga tcacgacctc tttagctttg cagatttgat ctttgggaag 660 tggcctgtgg ttcttatcac caatcctaaa tcactccttt atagttgtgg tgaacatgaa 720 ccactagaaa gacttcttca ctcaacacac atcagagtct tggccttttc cttatcctcc 780 attacttctg tcacagttaa gattgatgga gttcatttag gccaggctgt tcatgtgtct 840 ggtcccattt tcgtactgaa gtggaatcct agaaactaca gtagtgggac acataacata 900 gaagtaatcg tccaggattc tgctggaaga agtaagagtg ttcaccacat attttctgtt 960 caagagaata atcatctcag ttttgatccc ctggcatcat ttattctccg tactgatcac 1020 tacatcatgg cccgggtcct ttttgtgctg attgtgctga gccagctcac cattctcatt 1080 atttttagat atcgaggata cccagagctt aaaggtccat ggttttttgg tgaaatcatt 1140 gatggcaaat ttggttgctg cttttccttt gggatatttg ttaatggaca tttcctacaa 1200 ggcagcataa catttataat tggaattctc cagctggcgt tttttaacat ccccttgatg 1260 gcttacatgt gttggagctt gctgcagcgg tgctttggtc acaacttcag gtctcatctc 1320 catcaaagaa aatacttgaa aattatgcct gttcacctac ttatgctact gctgtacatc 1380 tggcaggttt attcctgcta ctttctttat gcaacatacg gcaccctagc ttttttattc 1440 tcccctttgc ggacctggtt gacactgctg acacctgttc tcattcgtta tgtgtggaca 1500 ctgaactcca ccaagtttgg aatcttcatg gtgcagttaa aaagccacct gagctcctga 1560 aggccatgtc tcaccactgg cagctgggca gaagcccagc ctctgtgtct gtagcccagg 1620 cctctacccc agtagcaggt ggagggccag gattggtggg tgagctttag ggagcagctg 1680 ctcgtttgga gtcctggacg ttggagggat tacccactac tgatacctgc agaatggact 1740 gcagaaaagt ctcaaaaata atgcctttat tccttccctc cctaaggagg caaagagttg 1800 atttaccttt gtgaagagaa aacccttatc taggacatcc acagggtaga ggttgggtgt 1860 gtgtacggga gtgtctgagg cccagtgtgt tttttagggt taccccatgt aaagcactta 1920 ccgctgtgct tggaattcag cagctgtcaa aggtgcaatt tcaggggcag ggaacctttg 1980 aggatctggg cccgaccctc actacccctg agatattagt tcccaggcct gttttcccac 2040 aggattgtgg gctctctgct tccttagtcg gaagtgtttt caactaatca aataaatgaa 2100 tgaatgatga ataagaaaaa acacagaccc aaaggggggg ccgccgaact atgggagcct 2160 cggtcgaccc ggggcaataa gttccggacc ggacccgtga cgggagtttt cccagacaac 2220 agggggaaga atatcgaatc gggcggtctt cccatatagt gcgctcgtat cacttgcgat 2280 aggccaggta acctgattag aaacctggga acaggcgaca caagccgaaa cagaacacac 2340 acacaacagg aagtgaccta acaccgtctg atagcgagtg cccacaacac acggcaacga 2400 cacacag 2407 <210> SEQ ID NO 86 <211> LENGTH: 1328 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Incyte ID No: 7504118CB1 <400> SEQUENCE: 86 gaattcggcg cgggctgcag acggctgcga ggcgctgggc acaggtgtcc tgatggcaaa 60 tttcaagggc cacgcgcttc cagggagttt cttcctgatc attgggctgt gttggtcagt 120 gaagtacccg ctgaagtact ttagccacac gcggaagaac agcccactac attactatca 180 gcgtctcgag atcgtcgaag ccgcaattag gactttgttt tccgtcactg gtttcctctt 240 ctactaccac gtccacaacc ggcctccgct ggaccagcac atccactcac tcctgctgta 300 tgctctgttc ggagggtgtg ttagtatctc cctagaggtg atcttccggg accacattgt 360 gctggaactt ttccgaacca gtctcatcat tcttcaggga acctggttct ggcagattgg 420 gtttgtgctg ttcccacctt ttggaacacc cgaatgggac cagaaggatg atgccaacct 480 catgttcatc accatgtgct tctgctggca ctacctggct gccctcagca ttgtggccgt 540 caactattct cttgtttact gccttttgac tcggatgaag agacacggaa ggggagaaat 600 cattggaatt cagaagctga attcagatga cacttaccag accgccctct tgagtggctc 660 agatgaggaa tgagccgaga tgcggagggc gcagatgtcc cactgcacag ctggaatgaa 720 tggagttcat cccctccacc tgaatgcctg ctgtggtctg atcttaaggg tctatatatt 780 tgcacctcct cattcaacac agggctggag gttctacaac aggaaatcag gcctacagca 840 tcctgtgtat cttgcagttg ggatttttaa acatactata aagtctgtgt tggtatagta 900 cccttcataa ggaaaaatga agtaatgcct ataagtagca ggcctttgtg cctcagtgtc 960 aagagaaatc aagagatgct aaaagcttta caatggaagt ggcctcatgg atgaatccgg 1020 ggtatgagcc caggagaacg tgctgctttt ggtaacttat ccctttttct cttaagaaag 1080 caggtacttt cttattagaa atatgttaga atgtgtaagc aaacgacagt gcctttagaa 1140 ttacaattct aacttacata ttttttgaaa gtaaaataat tcacaagctt tggtatttta 1200 aaattattgt taaacatatc ataactaatc ataccagggt actgcaatac cactgtttat 1260 aagtgacaaa attaggccaa aggtggtttt tttttaaatc aaggagcttg ttactggctc 1320 tactgaga 1328 

What is claimed is:
 1. An isolated polypeptide selected from the group consisting of: a) a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, b) a polypeptide comprising a naturally occurring amino acid sequence at least 90% identical to an amino acid sequence selected from the group consisting of SEQ ID NO:1-42, c) a polypeptide consisting essentially of a naturally occurring amino acid sequence at least 90% identical to the amino acid sequence of SEQ ID NO:43, d) a biologically active fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43, and e) an immunogenic fragment of a polypeptide having an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 2. An isolated polypeptide of claim 1 comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 3. An isolated polynucleotide encoding a polypeptide of claim
 1. 4. An isolated polynucleotide encoding a polypeptide of claim
 2. 5. An isolated polynucleotide of claim 4 comprising a polynucleotide sequence selected from the group consisting of SEQ ED NO:44-86.
 6. A recombinant polynucleotide comprising a promoter sequence operably linked to a polynucleotide of claim
 3. 7. A cell transformed with a recombinant polynucleotide of claim
 6. 8. A transgenic organism comprising a recombinant polynucleotide of claim
 6. 9. A method of producing a polypeptide of claim 1, the method comprising: a) culturing a cell under conditions suitable for expression of the polypeptide, wherein said cell is transformed with a recombinant polynucleotide, and said recombinant polynucleotide comprises a promoter sequence operably linked to a polynucleotide encoding the polypeptide of claim 1, and b) recovering the polypeptide so expressed.
 10. A method of claim 9, wherein the polypeptide comprises an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 11. An isolated antibody which specifically binds to a polypeptide of claim
 1. 12. An isolated polynucleotide selected from the group consisting of a) a polynucleotide comprising a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, b) a polynucleotide comprising a naturally occurring polynucleotide sequence at least 90% identical to a polynucleotide sequence selected from the group consisting of SEQ ID NO:44-86, c) a polynucleotide complementary to a polynucleotide of a), d) a polynucleotide complementary to a polynucleotide of b), and e) an RNA equivalent of a)-d).
 13. An isolated polynucleotide comprising at least 60 contiguous nucleotides of a polynucleotide of claim
 12. 14. A method of detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 12, the method comprising: a) hybridizing the sample with a probe comprising at least 20 contiguous nucleotides comprising a sequence complementary to said target polynucleotide in the sample, and which probe specifically hybridizes to said target polynucleotide, under conditions whereby a hybridization complex is formed between said probe and said target polynucleotide or fragments thereof, and b) detecting the presence or absence of said hybridization complex, and, optionally, if present, the amount thereof.
 15. A method of claim 14, wherein the probe comprises at least 60 contiguous nucleotides.
 16. A method of detecting a target polynucleotide in a sample, said target polynucleotide having a sequence of a polynucleotide of claim 12, the method comprising: a) amplifying said target polynucleotide or fragment thereof using polymerase chain reaction amplification, and b) detecting the presence or absence of said amplified target polynucleotide or fragment thereof, and, optionally, if present, the amount thereof.
 17. A composition comprising a polypeptide of claim 1 and a pharmaceutically acceptable excipient.
 18. A composition of claim 17, wherein the polypeptide comprises an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 19. A method for treating a disease or condition associated with decreased expression of functional REMAP, comprising administering to a patient in need of such treatment the composition of claim
 17. 20. A method of screening a compound for effectiveness as an agonist of a polypeptide of claim 1, the method comprising: a) exposing a sample comprising a polypeptide of claim 1 to a compound, and b) detecting agonist activity in the sample.
 21. A composition comprising an agonist compound identified by a method of claim 20 and a pharmaceutically acceptable excipient.
 22. A method for treating a disease or condition associated with decreased expression of functional REMAP, comprising administering to a patient in need of such treatment a composition of claim
 21. 23. A method of screening a compound for effectiveness as an antagonist of a polypeptide of claim 1, the method comprising: a) exposing a sample comprising a polypeptide of claim 1 to a compound, and b) detecting antagonist activity in the sample.
 24. A composition comprising an antagonist compound identified by a method of claim 23 and a pharmaceutically acceptable excipient.
 25. A method for treating a disease or condition associated with overexpression of functional REMAP, comprising administering to a patient in need of such treatment a composition of claim
 24. 26. A method of screening for a compound that specifically binds to the polypeptide of claim 1, the method comprising: a) combining the polypeptide of claim 1 with at least one test compound under suitable conditions, and b) detecting binding of the polypeptide of claim 1 to the test compound, thereby identifying a compound that specifically binds to the polypeptide of claim
 1. 27. A method of screening for a compound that modulates the activity of the polypeptide of claim 1, the method comprising: a) combining the polypeptide of claim 1 with at least one test compound under conditions permissive for the activity of the polypeptide of claim 1, b) assessing the activity of the polypeptide of claim 1 in the presence of the test compound, and c) comparing the activity of the polypeptide of claim 1 in the presence of the test compound with the activity of the polypeptide of claim 1 in the absence of the test compound, wherein a change in the activity of the polypeptide of claim 1 in the presence of the test compound is indicative of a compound that modulates the activity of the polypeptide of claim
 1. 28. A method of screening a compound for effectiveness in altering expression of a target polynucleotide, wherein said target polynucleotide comprises a sequence of claim 5, the method comprising: a) exposing a sample comprising the target polynucleotide to a compound, under conditions suitable for the expression of the target polynucleotide, b) detecting altered expression of the target polynucleotide, and c) comparing the expression of the target polynucleotide in the presence of varying amounts of the compound and in the absence of the compound.
 29. A method of assessing toxicity of a test compound, the method comprising: a) treating a biological sample containing nucleic acids with the test compound, b) hybridizing the nucleic acids of the treated biological sample with a probe comprising at least 20 contiguous nucleotides of a polynucleotide of claim 12 under conditions whereby a specific hybridization complex is formed between said probe and a target polynucleotide in the biological sample, said target polynucleotide comprising a polynucleotide sequence of a polynucleotide of claim 12 or fragment thereof, c) quantifying the amount of hybridization complex, and d) comparing the amount of hybridization complex in the treated biological sample with the amount of hybridization complex in an untreated biological sample, wherein a difference in the amount of hybridization complex in the treated biological sample is indicative of toxicity of the test compound.
 30. A diagnostic test for a condition or disease associated with the expression of REMAP in a biological sample, the method comprising: a) combining the biological sample with an antibody of claim 11, under conditions suitable for the antibody to bind the polypeptide and form an antibody:polypeptide complex, and b) detecting the complex, wherein the presence of the complex correlates with the presence of the polypeptide in the biological sample.
 31. The antibody of claim 11, wherein the antibody is: a) a chimeric antibody, b) a single chain antibody, c) a Fab fragment, d) a F(ab′)₂ fragment, or e) a humanized antibody.
 32. A composition comprising an antibody of claim 11 and an acceptable excipient.
 33. A method of diagnosing a condition or disease associated with the expression of REMAP in a subject, comprising administering to said subject an effective amount of the composition of claim
 32. 34. A composition of claim 32, wherein the antibody is labeled.
 35. A method of diagnosing a condition or disease associated with the expression of REMAP in a subject, comprising administering to said subject an effective amount of the composition of claim
 34. 36. A method of preparing a polyclonal antibody with the specificity of the antibody of claim 11, the method comprising: a) immunizing an animal with a polypeptide consisting of an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, or an immunogenic fragment thereof, under conditions to elicit an antibody response, b) isolating antibodies from said animal, and c) screening the isolated antibodies with the polypeptide, thereby identifying a polyclonal antibody which binds specifically to a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43.
 37. A polyclonal antibody produced by a method of claim
 36. 38. A composition comprising the polyclonal antibody of claim 37 and a suitable carrier.
 39. A method of making a monoclonal antibody with the specificity of the antibody of claim 11, the method comprising: a) immunizing an animal with a polypeptide consisting of an amino acid sequence selected from the group consisting of SEQ ID NO: 1-43, or an immunogenic fragment thereof, under conditions to elicit an antibody response, b) isolating antibody producing cells from the animal, c) fusing the antibody producing cells with immortalized cells to form monoclonal antibody-producing hybridoma cells, d) culturing the hybridoma cells, and e) isolating from the culture monoclonal antibody which binds specifically to a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 40. A monoclonal antibody produced by a method of claim
 39. 41. A composition comprising the monoclonal antibody of claim 40 and a suitable carrier.
 42. The antibody of claim 11, wherein the antibody is produced by screening a Fab expression library.
 43. The antibody of claim 11, wherein the antibody is produced by screening a recombinant immunoglobulin library.
 44. A method of detecting a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43 in a sample, the method comprising: a) incubating the antibody of claim 11 with a sample under conditions to allow specific binding of the antibody and the polypeptide, and b) detecting specific binding, wherein specific binding indicates the presence of a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43 in the sample.
 45. A method of purifying a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43 from a sample, the method comprising: a) incubating the antibody of claim 11 with a sample under conditions to allow specific binding of the antibody and the polypeptide, and b) separating the antibody from the sample and obtaining the purified polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1-43.
 46. A microarray wherein at least one element of the microarray is a polynucleotide of claim
 13. 47. A method of generating an expression profile of a sample which contains polynucleotides, the method comprising: a) labeling the polynucleotides of the sample, b) contacting the elements of the microarray of claim 46 with the labeled polynucleotides of the sample under conditions suitable for the formation of a hybridization complex, and c) quantifying the expression of the polynucleotides in the sample.
 48. An array comprising different nucleotides molecules affixed in distinct physical locations on a solid substrate, wherein at least one of said nucleotides molecules comprises a first oligonucleotide or polynucleotide sequence specifically hybridizable with at least 30 contiguous nucleotides of a target polynucleotide, and wherein said target polynucleotide is a polynucleotide of claim
 12. 49. An array of claim 48, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 30 contiguous nucleotides of said target polynucleotide.
 50. An array of claim 48, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to at least 60 contiguous nucleotides of said target polynucleotide.
 51. An array of claim 48, wherein said first oligonucleotide or polynucleotide sequence is completely complementary to said target polynucleotide.
 52. An array of claim 48, which is a microarray.
 53. An array of claim 48, further comprising said target polynucleotide hybridized to a nucleotides molecule comprising said first oligonucleotide or polynucleotide sequence.
 54. An array of claim 48, wherein a linker joins at least one of said nucleotides molecules to said solid substrate.
 55. An array of claim 48, wherein each distinct physical location on the substrate contains multiple nucleotide molecules, and the multiple nucleotide molecules at any single distinct physical location have the same sequence, and each distinct physical location on the substrate contains nucleotide molecules having a sequence which differs from the sequence of nucleotide molecules at another distinct physical location on the substrate.
 56. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:1.
 57. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:2.
 58. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:3.
 59. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:4.
 60. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:5.
 61. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:6.
 62. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:7.
 63. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:8.
 64. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:9.
 65. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:10.
 66. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:11.
 67. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:12.
 68. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:13.
 69. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:14.
 70. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:15.
 71. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:16.
 72. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:17.
 73. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:18.
 74. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:19.
 75. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:20.
 76. A polypeptide of claim 1, comprising tie amino acid sequence of SEQ ID NO:21.
 77. A polypeptide of claim 1, comprising (he amino acid sequence of SEQ ID NO:22.
 78. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:23.
 79. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:24.
 80. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:25.
 81. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:26.
 82. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:27.
 83. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:28.
 84. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:29.
 85. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:30.
 86. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:31.
 87. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:32.
 88. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:33.
 89. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:34.
 90. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:35.
 91. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:36.
 92. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:37.
 93. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:38.
 94. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:39.
 95. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:40.
 96. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:41.
 97. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:42.
 98. A polypeptide of claim 1, comprising the amino acid sequence of SEQ ID NO:43.
 99. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:44.
 100. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:45.
 101. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:46.
 102. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:47.
 103. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:48.
 104. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:49.
 105. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:50.
 106. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:51.
 107. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:52.
 108. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:53.
 109. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:54.
 110. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:55.
 111. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:56.
 112. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:57.
 113. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:58.
 114. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:59.
 115. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:60.
 116. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:61.
 117. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:62.
 118. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:63.
 119. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:64.
 120. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:65.
 121. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:66.
 122. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:67.
 123. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:68.
 124. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:69.
 125. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:70.
 126. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:71.
 127. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:72.
 128. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:73.
 129. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:74.
 130. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:75.
 131. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:76.
 132. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:77.
 133. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:78.
 134. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:79.
 135. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:80.
 136. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:81.
 137. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:82.
 138. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:83.
 139. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:84.
 140. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:85.
 141. A polynucleotide of claim 12, comprising the polynucleotide sequence of SEQ ID NO:86. 